Roxee Meds Catalog

Neomycin Sulfate

Medication catalog facts with explicit FDA-approval, off-label, source-limited, and safety context.

Both Catalog complete FDA data linked Rx required Powder for oral solution Multiple FDA labelers Official label facts Owner quick guide first

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Animal Drugs @ FDA: Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
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Animal Drugs @ FDA previews: Source FDA | Refreshed Feb 9, 2026, 3:05 AM UTC
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Package/product NDCs from FDA’s electronic listing directory (XLS).

Evidence

Reviewed / Updated / Sources

Reviewed by: Not available

Last reviewed: February 12, 2026

Updated: February 12, 2026, 10:44 PM UTC

Sources:

FDA application profile · official_label
FDA application profile · official_label
Medication usage source · fda_animal_drugs
Neomix® 325 Soluble Powder Neomix® AG 325 Soluble Powder · official_label
openFDA case USA-USFDACVM-2025-US-056132 · adverse_reaction

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Neomycin Sulfate

Drug type: Generic ingredient • Branded profile • FDA branded products available

Both Powder for oral solution Rx required 100% storefront ready

Species: Both

Manufacturer: Multiple FDA labelers

Medication Snapshot

Merged from the current Roxee medication system with field-level provenance, freshness, and completeness tracking.

Neomycin Sulfate

It is indicated for treating acute otitis externa and, to a lesser degree, chronic otitis externa in dogs. In treatment of ear canker and other inflammatory conditions of the external ear canal. It is indicated for treating acute otitis externa and, to a lesser degree, chronic otitis externa in cats. In treatment of ear canker and other inflammatory conditions of the external ear canal. For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle. Species commonly shown: Both, Goat, No Use Class Stated Or Implied, No use class stated or implied.

Generic name

Neomycin Sulfate

Brand names

Neomix® 325 Soluble Powder Neomix® AG 325 Soluble Powder, Neomix Ag® 325 Neomix® 325, Neomycin Sulfate, NeoMed® Soluble Powder

Manufacturer

Multiple FDA labelers

Species

Both, Goat, No Use Class Stated Or Implied, No use class stated or implied, Excluding veal calves or female dairy cattle 20 months of age or older

Dosage forms

Powder for oral solution, Type A Medicated Article, Soluble Powder, Liquid (Solution)

Prescription

Prescription required

Completeness

100%

Validation

Complete

Brand names

Neomix® 325 Soluble Powder Neomix® AG 325 Soluble Powder Neomix Ag® 325 Neomix® 325 Neomycin Sulfate NeoMed® Soluble Powder Biosol® Liquid Neomycin Oral Solution Neo-Sol® 50 Neo 200 Oral Solution Neosol Soluble Powder Neosol-Oral Neomycin Sulfate 325 Neomycin Liquid Biosol® Sterile Solution Biosol® Sterile Solution 50 mg Neomycane Ophthalmic Ointment Neoplex Neo-Sol 50 Neomycin NeoMed 325 Neovet NEOSOL

Dosage forms

Powder for oral solution Type A Medicated Article Soluble Powder Liquid (Solution) Ointment

Indications / Uses

Warnings / Contraindications

Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product. If such signs are noted, therapy with the product should be stopped. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues.

Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product. If such signs are noted, therapy with the product should be stopped. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues.

Side Effects

Top reported reactions (openFDA): Lethargy (see also Central nervous system depression in 'Neurological'), Loss of hearing, Deafness, Lack of efficacy - NOS, Vomiting, Pinnal erythema.

FAQ

Both, Goat, No Use Class Stated Or Implied, No use class stated or implied, Excluding veal calves or female dairy cattle 20 months of age or older, Growing, Sheep, No Use Class Stated Or Implied, Goats, excluding lactating goats, excluding dairy females 12 months of age or older, Kids, Baby Pigs, Excluding lactating dairy, excluding dairy females 20 months of age or older, Calves, excluding veal calves, Lambs, Cattle, Excluding Veal Calves, Dog, No Use Class Stated Or Implied, Cat, No Use Class Stated Or Implied

Yes. Roxee shows this as prescription-only.

Powder for oral solution, Type A Medicated Article, Soluble Powder, Liquid (Solution)

Related Conditions

Otitis Externa (Ear Infection)

Source Transparency

Verified source: https://www.roxee.ai/meds/
Verified source: https://animaldrugsatfda.fda.gov
Verified source: https://animaldrugsatfda.fda.gov/adafda/views/#/search
Verified source: https://api.fda.gov/animalandveterinary/event.json
Verified source: https://www.roxee.ai/conditions/
Verified source: https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/984
Last refreshed: May 5, 2026, 10:00 a.m.
Last verified: Feb 12, 2026, 10:44 p.m.
Validation status: Complete

Add to My Pet's Meds

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Pet Owner Quick Guide

Start here first for the safest next-step summary before the deeper medication detail.

Used for:

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosing note:

Exact dosing depends on your pet's species, weight, and health status. Use your veterinarian's instructions for the exact dose and schedule.

What to watch for:

Tetracaine and neomycin have the potential to sensitize
Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product
If such signs are noted, therapy with the product should be stopped
Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia
Add to drinking water
Not for use in liquid supplements
Prepare a fresh solution daily
If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian
Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days
Discontinue treatment 1 day prior to slaughter in cattle
A withdrawal period has not been established for use in preruminating calves
Do not use in calves to be processed for veal
Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues
Discontinue treatment 2 days prior to slaughter in sheep
Gall bladder inflammation (1 reports)
Found dead (1 reports)
Elevated total bilirubin (1 reports)

When to call the vet:

Repeated vomiting or diarrhea.
Severe lethargy (hard to wake, very low energy).
Collapse or fainting.
Trouble breathing.
Facial swelling or hives.
Blood in vomit or stool.

Regulatory restrictions are shown in Vet View.

What to tell or ask your vet today:

Is this medicine the right fit for my pet’s current symptoms?
Which warning signs mean I should call back right away?
How should I handle missed doses or refusal to take the medicine?

Major cautions & emergency warning signs

Side effects to monitor:

Tetracaine and neomycin have the potential to sensitize
Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product
If such signs are noted, therapy with the product should be stopped
Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia
Add to drinking water

Most reported reactions:

Gall bladder inflammation (1 reports)
Found dead (1 reports)
Elevated total bilirubin (1 reports)

Emergency warning signs:

Repeated vomiting or diarrhea.
Severe lethargy (hard to wake, very low energy).
Collapse or fainting.
Trouble breathing.

Talk to a Vet / Find a Vet Near You Start Symptom Intake

Quick Facts

Official label facts first, then secondary summaries. Marketing content is separated below.

Species: Both

Manufacturer: Multiple FDA labelers

Form: Liquid (Solution), Ointment, Powder for oral solution, Soluble Powder, Type A Medicated Article

Identifiers:

ANADA: 200046 ANADA: 200050 ANADA: 200113 ANADA: 200118 ANADA: 200130 ANADA: 200153 ANADA: 200235 ANADA: 200245 ANADA: 200289 ANADA: 200330 ANADA: 200378 ANADA: 200379 ANADA: 200553 ANADA: 200565 NADA: 10524 NADA: 11315 NADA: 11437 NADA: 11703 NADA: 11953 NADA: 12258

Source metadata:

https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/200235 · official_label · FDA application profile
https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/140976 · official_label · FDA application profile
https://animaldrugsatfda.fda.gov · fda_animal_drugs · Medication usage source

Warnings / Contraindications

High: Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product. If such signs are noted, therapy with the product should be stopped. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues.

Source metadata:

https://animaldrugsatfda.fda.gov · fda_animal_drugs · Contraindication source

Adverse Reactions

Snapshot first, detailed rows second. This section summarizes signal data and is not a diagnosis.

Tap or hover a reaction to see what it means in plain language.

Tracked signals

Reported cases

Serious reports

Species represented

Grouped by Body System

Digestive (3) · Loss of appetite, Diarrhea, Decreased appetite Skin & allergy (1) · Ear flapping/twitching Neurologic (2) · Unsteady walking (ataxia), Circling - neurological disorder Other (26) · Gall bladder inflammation, Found dead, Flaking skin

Most Reported Reactions

Body system	Cases	Species	Serious cases
Other	1	Cat	1
Other	1	Dog	1
Other	1	Cat	1
Other	1	Cat	1
Other	1	Cat	1
Other	1	Cat	1
Skin & allergy	1	Dog	1
Digestive	1	Dog	1

Species coverage: Dog (17) Cat (15)

View detailed reaction table

Body system	Species	Seriousness	Frequency	Reports
Neurologic	Cat	Non-serious	-	1
Digestive	Cat	Non-serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Serious	-	1
Other	Cat	Non-serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Non-serious	-	1
Other	Cat	Serious	-	1
Other	Cat	Serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Non-serious	-	1
Skin & allergy	Dog	Serious	-	1
Other	Dog	Non-serious	-	1
Other	Dog	Non-serious	-	1
Digestive	Dog	Serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Non-serious	-	1
Other	Dog	Non-serious	-	1
Digestive	Cat	Non-serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Non-serious	-	1
Other	Dog	Serious	-	1
Neurologic	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Dog	Serious	-	1
Other	Cat	Serious	-	1
Other	Dog	Non-serious	-	1
Other	Cat	Serious	-	1
Other	Cat	Non-serious	-	1
Other	Cat	Non-serious	-	1

Source metadata:

https://api.fda.gov/animalandveterinary/event.json · adverse_reaction · openFDA case USA-USFDACVM-2025-US-056132

Documents

Owner handouts and official technical documents open on-page first, with the original source still one click away.

Owner handouts

No owner handouts linked yet.

Official label / PI

SPL

FOI

011-315

Official label / PI · EA

Open original

011-315

Official label / PI · FONSI

Open original

011-315

Official label / PI · EA

Open original

011-315

Official label / PI · FONSI

Open original

Neosol Soluble Powder

SPL · SPL

Open original

FDA Structured Product Label

Neosol Soluble Powder

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Dechra Veterinary Products LLC
ANADA: 200-235
Status: RX
Form: Liquid (Solution)
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Withdraw 1 day before slaughter.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Neomix Ag® 325

SPL · SPL

Open original

FDA Structured Product Label

Neomix Ag® 325 Neomix® 325

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Phibro Animal Health Corp.
NADA: 140-976
Status: VFD
Form: Type A Medicated Article
Route: Oral
Species: Goats, excluding lactating goats, excluding dairy females 12 months of age or older • Kids • Baby Pigs • No use class stated or implied • Excluding lactating dairy, excluding dairy females 20 months of age or older • Calves, excluding veal calves • Sheep, No Use Class Stated Or Implied • Lambs

Composition / specifications

325 g neomycin sulfate per lb

Cattle, swine, sheep, and goats, and their offspring

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle, swine, sheep, goats and their offspring.

Dosage

Type C milk replacer 400 to 2,000 grams per ton.

Type C feed 250 to 2,500 grams per ton.

Neomix® 325

SPL · SPL

Open original

FDA Structured Product Label

Neomix Ag® 325 Neomix® 325

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Phibro Animal Health Corp.
NADA: 140-976
Status: VFD
Form: Type A Medicated Article
Route: Oral
Species: Goats, excluding lactating goats, excluding dairy females 12 months of age or older • Kids • Baby Pigs • No use class stated or implied • Excluding lactating dairy, excluding dairy females 20 months of age or older • Calves, excluding veal calves • Sheep, No Use Class Stated Or Implied • Lambs

Composition / specifications

325 g neomycin sulfate per lb

Cattle, swine, sheep, and goats, and their offspring

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle, swine, sheep, goats and their offspring.

Dosage

Type C milk replacer 400 to 2,000 grams per ton.

Type C feed 250 to 2,500 grams per ton.

Neomix® 325 Soluble Powder

SPL · SPL

Open original

FDA Structured Product Label

Neomix® 325 Soluble Powder Neomix® AG 325 Soluble Powder

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Phibro Animal Health Corp.
NADA: 11315
Status: RX
Form: Powder for oral solution
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Excluding veal calves or female dairy cattle 20 months of age or older • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves or female dairy cattle 20 months of age or older)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Turkeys (growing)

Indication

For the control of mortality associated with E. coli organisms susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Neomix® AG 325 Soluble Powder

SPL · SPL

Open original

FDA Structured Product Label

Neomix® 325 Soluble Powder Neomix® AG 325 Soluble Powder

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Phibro Animal Health Corp.
NADA: 11315
Status: RX
Form: Powder for oral solution
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Excluding veal calves or female dairy cattle 20 months of age or older • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves or female dairy cattle 20 months of age or older)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Turkeys (growing)

Indication

For the control of mortality associated with E. coli organisms susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Neomycin Sulfate

SPL · SPL

Open original

FDA Structured Product Label

Neomycin Sulfate

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Phibro Animal Health Corp.
ANADA: 200-046
Status: RX
Form: Soluble Powder
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add powder to drinking water or milk; not for use in liquid supplements. Prepare a fresh solution in drinking water daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add powder to drinking water or milk; not for use in liquid supplements. Prepare a fresh solution in drinking water daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add powder to drinking water or milk; not for use in liquid supplements. Prepare a fresh solution in drinking water daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add powder to drinking water or milk; not for use in liquid supplements. Prepare a fresh solution in drinking water daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Neosol-Oral

SPL · SPL

Open original

FDA Structured Product Label

Neosol-Oral

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Med-Pharmex, Inc.
ANADA: 200-289
Status: RX
Form: Liquid (Solution)
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle (not for use in veal calves).

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys (growing)

Indication

For the control of mortality associated with E. coli organisms susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

NeoMed® Soluble Powder

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FDA Structured Product Label

NeoMed® Soluble Powder

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Bimeda Animal Health Limited
ANADA: 200-050
Status: RX
Form: Liquid (Solution)
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each ounce of powder contains 20.3 grams of neomycin sulfate (equivalent to 14.2 grams of neomycin base).

Turkeys (growing)

Indication

For the control of mortality associated with E. coli organisms susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 5 consecutive days. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Neomycin Oral Solution

SPL · SPL

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FDA Structured Product Label

Neomycin Oral Solution

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Huvepharma EOOD
ANADA: 200-118
Status: RX
Form: Liquid (Solution)
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base).

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day(22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

Amount: 10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neo 200 Oral Solution

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FDA Structured Product Label

Neo 200 Oral Solution

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Sponsor: Huvepharma EOOD
ANADA: 200-153
Status: RX
Form: Liquid (Solution)
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base).

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterialenteritis) caused by Escherichia coli susceptible to neomycin sulfate incattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Biosol® Liquid

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FDA Structured Product Label

Biosol® Liquid

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Sponsor: Zoetis Inc.
ANADA: 200-113
Status: RX
Form: Liquid (Solution)
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base).

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 1 day prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 2 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Liquid

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FDA Structured Product Label

Neomycin Liquid

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Sponsor: Sparhawk Laboratories, Inc.
ANADA: 200-379
Status: RX
Form: Liquid (Solution)
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base)

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Sulfate 325

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FDA Structured Product Label

Neomycin Sulfate 325

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Sparhawk Laboratories, Inc.
ANADA: 200-378
Status: RX
Form: Soluble Powder
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys (growing)

Indication

For the control of mortality associated with E. coli susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Neo-Sol® 50

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FDA Structured Product Label

Neo-Sol® 50

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Huvepharma EOOD
ANADA: 200-130
Status: RX
Form: Soluble Powder
Route: Oral
Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission ofdisease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days before slaughter.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys (growing)

Indication

For the control of mortality associated with Escherichia coli organisms susceptible to neomycin sulfate in growing turkeys.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Biosol® Sterile Solution

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FDA Structured Product Label

Biosol® Sterile Solution Biosol® Sterile Solution 50 mg

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Sponsor: Zoetis Inc.
NADA: 11953
Status: RX
Form: Liquid (Solution)
Route: Intramuscular, Intravenous
Species: Dog, No Use Class Stated Or Implied • Cat, No Use Class Stated Or Implied

Composition / specifications

Each milliliter of sterile aqueous solution contains 50 milligrams of neomycin sulfate (equivalent to 35 milligrams of neomycin base).

Cats

Indication

Administer to cats for the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.

Dosage

5 milligrams per pound of body weight daily divided into portions administered every 6 to 8 hours for 3 to 5 days. For intramuscular or intravenous use.

Limitations

Neomycin is not for use parenterally in food-producing animals because of prolonged residues in edible tissues. Labeling shall bear an appropriate expiration date. For use by or on the order of a licensed veterinarian.

Dogs

Indication

Administer to dogs for the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.

Dosage

5 milligrams per pound of body weight daily divided into portions administered every 6 to 8 hours for 3 to 5 days. For intramuscular or intravenous use.

Limitations

Biosol® Sterile Solution 50 mg

SPL · SPL

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FDA Structured Product Label

Biosol® Sterile Solution Biosol® Sterile Solution 50 mg

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor: Zoetis Inc.
NADA: 11953
Status: RX
Form: Liquid (Solution)
Route: Intramuscular, Intravenous
Species: Dog, No Use Class Stated Or Implied • Cat, No Use Class Stated Or Implied

Composition / specifications

Each milliliter of sterile aqueous solution contains 50 milligrams of neomycin sulfate (equivalent to 35 milligrams of neomycin base).

Cats

Indication

Administer to cats for the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.

Dosage

5 milligrams per pound of body weight daily divided into portions administered every 6 to 8 hours for 3 to 5 days. For intramuscular or intravenous use.

Limitations

Dogs

Indication

Administer to dogs for the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.

Dosage

5 milligrams per pound of body weight daily divided into portions administered every 6 to 8 hours for 3 to 5 days. For intramuscular or intravenous use.

Limitations

Neomycane Ophthalmic Ointment

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FDA Structured Product Label

Neomycane Ophthalmic Ointment

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Sponsor: Evsco Pharmaceuticals, An Affiliate of IGI, Inc.
NADA: 44655
Status: OTC
Form: Ointment
Route: Ophthalmic
Species: Dog, No Use Class Stated Or Implied • Cat, No Use Class Stated Or Implied

Composition / specifications

Each gram of the ointment contains 5 milligrams of neomycin sulfate equivalent in activity to 3.5 milligrams of neomycin base.

Dogs

Indication

The drug is intended for use in dogs for the treatment of superficial ocular bacterial infections limited to the conjunctival or the anterior segment of the eye.

Dosage

The drug is applied four times each day.

Limitations

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Cats

Indication

The drug is intended for use in cats for the treatment of superficial ocular bacterial infections limited to the conjunctival or the anterior segment of the eye.

Dosage

The drug is applied four times each day.

Limitations

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Neomycin Sulfate SPL

SPL · Structured Product Label

Open original

FDA Structured Product Label XML for Neomycin Sulfate. Use the source link for the full official labeling record.

Neomycin Sulfate SPL

SPL · Structured Product Label

Open original

FDA Structured Product Label XML for Neomycin Sulfate. Use the source link for the full official labeling record.

Neomycin Sulfate SPL

SPL · Structured Product Label

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FDA Structured Product Label XML for Neomycin Sulfate. Use the source link for the full official labeling record.

Neovet SPL

SPL · Structured Product Label

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FDA Structured Product Label XML for Neovet. Use the source link for the full official labeling record.

NEOSOL SPL

SPL · Structured Product Label

Open original

FDA Structured Product Label XML for NEOSOL. Use the source link for the full official labeling record.

Neo-Sol 50 SPL

SPL · Structured Product Label

Open original

FDA Structured Product Label XML for Neo-Sol 50. Use the source link for the full official labeling record.

NeoMed 325 SPL

SPL · Structured Product Label

Open original

FDA Structured Product Label XML for NeoMed 325. Use the source link for the full official labeling record.

Neomycin SPL

SPL · Structured Product Label

Open original

FDA Structured Product Label XML for Neomycin. Use the source link for the full official labeling record.

Neomycin SPL

SPL · Structured Product Label

Open original

FDA Structured Product Label XML for Neomycin. Use the source link for the full official labeling record.

Neoplex SPL

SPL · Structured Product Label

Open original

FDA Structured Product Label XML for Neoplex. Use the source link for the full official labeling record.

A200235_Orig_3_9_1998.pdf

FOI · FOI

Open original

ucm115965.pdf

FOI · FOI

Open original

ucm049525.pdf

FOI · FOI

Open original

N011315_Supp_4_3_1996.pdf

FOI · FOI

Open original

UCM523941.pdf

FOI · FOI

Open original

A200046_Supp_04_03_1996.pdf

FOI · FOI

Open original

A200046_Orig_05_15_1992.pdf

FOI · FOI

Open original

ucm061717.pdf

FOI · FOI

Open original

ucm061573.pdf

FOI · FOI

Open original

A200050_Supp_04_03_1996.pdf

FOI · FOI

Open original

A200050_Orig_02_15_1995.pdf

FOI · FOI

Open original

A200118_Supp_7_14_1998.pdf

FOI · FOI

Open original

A200118_Orig_11_29_1994..pdf

FOI · FOI

Open original

A200153_Orig_05_08_1996.pdf

FOI · FOI

Open original

A200113_Supp_02_07_1997.pdf

FOI · FOI

Open original

A200113_Org_6_28_1993.pdf

FOI · FOI

Open original

ucm061334.pdf

FOI · FOI

Open original

ucm061332.pdf

FOI · FOI

Open original

ucm061598.pdf

FOI · FOI

Open original

N140810_Org_5_31_1988.pdf

FOI · FOI summary

Open original

ucm061671.pdf

FOI · FOI summary

Open original

UCM457307.pdf

FOI · FOI summary

Open original

ucm061795.pdf

FOI · FOI summary

Open original

N140879_Org_8_2_1989.pdf

FOI · FOI summary

Open original

N140847_Org_9_30_1988.pdf

FOI · FOI summary

Open original

UCM457231.pdf

FOI · FOI summary

Open original

Source metadata:

https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1912 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/509/Neosol%20Soluble%20Powder · document · SPL
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/545 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/1194/Neomix%20Ag%C2%AE%20325 · document · SPL
https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/1195/Neomix%C2%AE%20325 · document · SPL
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/286 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1281 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/285 · document · FOI
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadEA/153 · document · EA
https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFonsi/156 · document · FONSI

Veterinary reference (advanced)

Canonical medication sections are above. This legacy block remains available for deeper cross-reference without cluttering the primary workflow.

At a Glance

Quick facts and links to official labeling and safety signals.

Data freshness

Storefront facts: Source Roxee | Refreshed May 5, 2026, 10:00 AM UTC
The storefront fact projection used for browse cards and quick facts.
Animal Drugs @ FDA: Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
Applications/products are imported from FDA export data.
Animal Drugs @ FDA previews: Source FDA | Refreshed Feb 9, 2026, 3:05 AM UTC
Label highlights/doc links are fetched from FDA preview endpoints.
Animal Drug Product Listing Directory (NDC): Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
Package/product NDCs from FDA’s electronic listing directory (XLS).

Official (FDA)

Identity: Generic ingredient • FDA branded products available

Official FDA brands: NEOSOL Neo-Sol 50 NeoMed 325 Neomycin Neomycin Sulfate Neoplex Neovet

Manufacturer mapping: Multiple FDA labelers

Catalog species: Both • FDA-labeled species: Baby Pigs, Calves, Cat, Cattle, Dog, Excluding lactating dairy, Excluding veal calves or female dairy cattle 20 months of age or older, Goat, Goats, Growing, Kids, Lambs, No use class stated or implied, Sheep

Rx/OTC: OTC, RX, VFD

Form/route: Liquid (Solution), Ointment, Powder for oral solution, Soluble Powder, Type A Medicated Article • Intramuscular, Intravenous, Ophthalmic, Oral

Applications: ANADA 200-235 • NADA 140-976 • NADA 11315 • ANADA 200-046 • ANADA 200-289 • ANADA 200-050 • ANADA 200-118 • ANADA 200-153 • ANADA 200-113 • ANADA 200-379 • ANADA 200-378 • ANADA 200-130 • NADA 11953 • NADA 44655

NDC: Packages 13985-578-01 13985-578-16 17033-417-50 23243-6755-1 23243-6755-2 23243-6755-3 • Products 13985 17033 23243 43457 46066 55999

Documents: 23 (FOI: 19) • SPL: 17 • Label highlights • Official documents

Safety (openFDA)

Top reactions: Dog 0 • Cat 0 • View

Case summaries: 0

openFDA reports are unverified and do not prove causation.

Explore

Related conditions: Otitis Externa (Ear Infection)

Linked using: Usage_Inferred (0.78)

Diagnosis Codes

ICD10_CM: A27.9 ICD10_CM: H60.90 ICD10_CM: L20.9

Leptospirosis, unspecified

Counseling and Monitoring Highlights

Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.

Owner-facing counseling points

Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to the product. If such signs are noted, therapy with the product should be stopped. Incomplete response or exacerbation of corticosteroid responsive lesions may be due to the presence of non susceptible organisms or to prolonged use of antibiotic-containing preparations resulting in overgrowth of non susceptible organisms, particularly Monilia. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. (Contraindication, High)

Top reaction signals

Gall bladder inflammation (1) Found dead (1) Elevated total bilirubin (1) Elevated serum alkaline phosphatase (1) Elevated gamma-glutamyl transferase (1) Elevated alanine aminotransferase (1) Ear flapping/twitching (1) Diarrhea (1)

Identifiers & Packages

Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.

Identifiers

Package NDC	Product NDC	Status
0010-5587-01	0010	-
0010-5587-02	0010	-
0010-5587-03	0010	-
0010-5587-04	0010	-
13985-578-01	13985	-
13985-578-16	13985	-
17033-122-15	17033	-
17033-122-30	17033	-
17033-122-75	17033	-
17033-417-50	17033	-
23243-6755-1	23243	-
23243-6755-2	23243	-
23243-6755-3	23243	-
43457-538-25	43457	-
46066-211-05	46066	-
46066-211-07	46066	-
51429-010-03	51429	-
51429-055-03	51429	-
54771-1584-1	54771	-
55999-069-13	55999	-

Enriched Documents

Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.

Neomycin Sulfate SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Neomycin Sulfate SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Neomycin Sulfate SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Neovet SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
NEOSOL SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Neo-Sol 50 SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
NeoMed 325 SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Neomycin SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Neomycin SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
Neoplex SPL • Structured Product Label • Official
FDA Structured Product Label from the electronic animal drug product listing directory.
A200235_Orig_3_9_1998.pdf • FOI summary • Official • Feb. 27, 2026
FDA FOI summary for application 200235
ucm115965.pdf • FOI summary • Official • July 30, 2025
FDA FOI summary for application 140976
UCM523941.pdf • FOI summary • Official • July 2, 2025
FDA FOI summary for application 11315
N011315_Supp_4_3_1996.pdf • FOI summary • Official • July 2, 2025
FDA FOI summary for application 11315
ucm049525.pdf • FOI summary • Official • July 2, 2025
FDA FOI summary for application 11315
N140810_Org_5_31_1988.pdf • FOI summary • Official • Jan. 21, 2025
FDA FOI summary for application 140810
A200046_Orig_05_15_1992.pdf • FOI summary • Official • Nov. 12, 2024
FDA FOI summary for application 200046
A200046_Supp_04_03_1996.pdf • FOI summary • Official • Nov. 12, 2024
FDA FOI summary for application 200046
ucm061717.pdf • FOI summary • Official • Dec. 26, 2023
FDA FOI summary for application 200289
ucm061671.pdf • FOI summary • Official • Dec. 26, 2023
FDA FOI summary for application 200245
UCM457307.pdf • FOI summary • Official • Oct. 25, 2023
FDA FOI summary for application 200553
A200050_Orig_02_15_1995.pdf • FOI summary • Official • Oct. 2, 2018
FDA FOI summary for application 200050
A200050_Supp_04_03_1996.pdf • FOI summary • Official • Oct. 2, 2018
FDA FOI summary for application 200050
ucm061573.pdf • FOI summary • Official • Oct. 2, 2018
FDA FOI summary for application 200050
ucm061795.pdf • FOI summary • Official • Dec. 27, 2017
FDA FOI summary for application 200330
A200118_Orig_11_29_1994..pdf • FOI summary • Official • Dec. 13, 2017
FDA FOI summary for application 200118
A200118_Supp_7_14_1998.pdf • FOI summary • Official • Dec. 13, 2017
FDA FOI summary for application 200118
A200153_Orig_05_08_1996.pdf • FOI summary • Official • July 28, 2017
FDA FOI summary for application 200153
A200113_Org_6_28_1993.pdf • FOI summary • Official • May 19, 2017
FDA FOI summary for application 200113
A200113_Supp_02_07_1997.pdf • FOI summary • Official • May 19, 2017
FDA FOI summary for application 200113
N140879_Org_8_2_1989.pdf • FOI summary • Official • May 17, 2017
FDA FOI summary for application 140879
N140847_Org_9_30_1988.pdf • FOI summary • Official • May 17, 2017
FDA FOI summary for application 140847
ucm061334.pdf • FOI summary • Official • Jan. 3, 2017
FDA FOI summary for application 200379
ucm061332.pdf • FOI summary • Official • Jan. 3, 2017
FDA FOI summary for application 200378
ucm061598.pdf • FOI summary • Official • Jan. 3, 2017
FDA FOI summary for application 200130
UCM457231.pdf • FOI summary • Official • June 1, 2016
FDA FOI summary for application 200565

Data Sources & Change Log

Every non-trivial field is expected to include provenance and update timestamps.

Official 73 Clinical 2 Manufacturer 0 Marketing 0

Current Field Facts

side_effects: Top reported reactions (openFDA): Lethargy (see also Central nervous system depression in 'Neurological'), Loss of hearing, Deafness, Lack of efficacy - NOS, V… (Clinical, 2026-05-02)
side_effects: Top reported reactions (openFDA): Lethargy (see also Central nervous system depression in 'Neurological'), Loss of hearing, Deafness, Lack of efficacy - NOS, V… (Clinical, 2026-04-11)
contraindications: Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to t… (Official, 2026-05-02)
contraindications: Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to t… (Official, 2026-04-30)
contraindications: Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to t… (Official, 2026-04-11)
contraindications: Tetracaine and neomycin have the potential to sensitize. Care should be taken to observe animals being treated for evidence of hypersensitivity or allergy to t… (Official, 2026-02-12)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-05-05)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-05-03)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-05-02)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-04-29)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-04-28)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-04-27)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-04-26)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-04-25)
indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calv… (Official, 2026-04-22)
manufacturer_name: Multiple FDA labelers (Official, 2026-05-05)
manufacturer_name: Multiple FDA labelers (Official, 2026-05-03)
manufacturer_name: Multiple FDA labelers (Official, 2026-05-02)
manufacturer_name: Multiple FDA labelers (Official, 2026-04-29)
manufacturer_name: Multiple FDA labelers (Official, 2026-04-28)

Recent Revisions

side_effects updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
contraindications updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
usage updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
side_effects updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
contraindications updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
usage updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
side_effects updated 2026-04-11 10:05 by etl_backfill • Backfilled from existing medication fields
contraindications updated 2026-04-11 10:05 by etl_backfill • Backfilled from existing medication fields
usage updated 2026-04-11 10:05 by etl_backfill • Backfilled from existing medication fields
side_effects updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
contraindications updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
usage updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields

FDA Products & Applications (Animal Drugs @ FDA)

Official sponsor/proprietary-name/application-status records linked by active ingredient.

Product	Sponsor	Application	Status	Published
Neosol Soluble Powder RX Neomycin Sulfate Liquid (Solution) • Oral Label highlights Official documents	Dechra Veterinary Products LLC	ANADA 200-235	Approved	Feb 27, 2026
Neomix Ag® 325 Neomix® 325 VFD Neomycin Sulfate Type A Medicated Article • Oral Label highlights Official documents	Phibro Animal Health Corp.	NADA 140-976	Approved	Jul 30, 2025
Neomix® 325 Soluble Powder Neomix® AG 325 Soluble Powder RX Neomycin Sulfate Powder for oral solution • Oral Label highlights Official documents	Phibro Animal Health Corp.	NADA 11315	Approved	Jul 2, 2025
Neomycin Sulfate RX Neomycin Sulfate Soluble Powder • Oral Label highlights Official documents	Phibro Animal Health Corp.	ANADA 200-046	Approved	Nov 12, 2024
Neosol-Oral RX Neomycin Sulfate Liquid (Solution) • Oral Label highlights Official documents	Med-Pharmex, Inc.	ANADA 200-289	W	Dec 26, 2023
NeoMed® Soluble Powder RX Neomycin Sulfate Liquid (Solution) • Oral Label highlights Official documents	Bimeda Animal Health Limited	ANADA 200-050	Approved	Oct 2, 2018
Neomycin Oral Solution RX Neomycin Sulfate Liquid (Solution) • Oral Label highlights Official documents	Huvepharma EOOD	ANADA 200-118	Approved	Dec 13, 2017
Neo 200 Oral Solution RX Neomycin Sulfate Liquid (Solution) • Oral Label highlights Official documents	Huvepharma EOOD	ANADA 200-153	Approved	Jul 28, 2017
Biosol® Liquid RX Neomycin Sulfate Liquid (Solution) • Oral Label highlights Official documents	Zoetis Inc.	ANADA 200-113	Approved	May 19, 2017
Neomycin Liquid RX Neomycin Sulfate Liquid (Solution) • Oral Label highlights Official documents	Sparhawk Laboratories, Inc.	ANADA 200-379	Approved	Jan 3, 2017
Neomycin Sulfate 325 RX Neomycin Sulfate Soluble Powder • Oral Label highlights Official documents	Sparhawk Laboratories, Inc.	ANADA 200-378	Approved	Jan 3, 2017
Neo-Sol® 50 RX Neomycin Sulfate Soluble Powder • Oral Label highlights Official documents	Huvepharma EOOD	ANADA 200-130	Approved	Jan 3, 2017
Biosol® Sterile Solution Biosol® Sterile Solution 50 mg RX Neomycin Sulfate Liquid (Solution) • Intramuscular, Intravenous Label highlights Official documents	Zoetis Inc.	NADA 11953	Approved	Jun 1, 2016
Neomycane Ophthalmic Ointment OTC Neomycin Sulfate Ointment • Ophthalmic Label highlights Official documents	Evsco Pharmaceuticals, An Affiliate of IGI, Inc.	NADA 44655	W	Jun 1, 2016

Data source: FDA Animal Drugs @ FDA (public search export).

What It's For (FDA Label Highlights)

Extracted from FDA Animal Drugs @ FDA product labeling. Always confirm details with your veterinarian.

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Goats, excluding lactating goats, excluding dairy females 12 months of age or older • Kids • Baby Pigs • No use class stated or implied • Excluding lactating dairy, excluding dairy females 20 months of age or older • Calves, excluding veal calves • Sheep, No Use Class Stated Or Implied • Lambs

Composition / specifications

325 g neomycin sulfate per lb

Cattle, swine, sheep, and goats, and their offspring

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle, swine, sheep, goats and their offspring.

Dosage

Type C milk replacer 400 to 2,000 grams per ton.

Type C feed 250 to 2,500 grams per ton.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Excluding veal calves or female dairy cattle 20 months of age or older • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves or female dairy cattle 20 months of age or older)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Turkeys (growing)

Indication

For the control of mortality associated with E. coli organisms susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add powder to drinking water or milk; not for use in liquid supplements. Prepare a fresh solution in drinking water daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add powder to drinking water or milk; not for use in liquid supplements. Prepare a fresh solution in drinking water daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add powder to drinking water or milk; not for use in liquid supplements. Prepare a fresh solution in drinking water daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 1 day prior to slaughter in cattle (not for use in veal calves).

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys (growing)

Indication

For the control of mortality associated with E. coli organisms susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each ounce of powder contains 20.3 grams of neomycin sulfate (equivalent to 14.2 grams of neomycin base).

Turkeys (growing)

Indication

For the control of mortality associated with E. coli organisms susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 5 consecutive days. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base).

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day(22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

Amount: 10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base).

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterialenteritis) caused by Escherichia coli susceptible to neomycin sulfate incattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base).

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 2 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Sheep, No Use Class Stated Or Implied

Composition / specifications

Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base)

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in cattle (excluding veal calves).

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in sheep.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 2 days prior to slaughter in sheep. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in swine.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in swine. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate in goats.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days.

Limitations

Add to drinking water. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 days. Discontinue treatment 3 days prior to slaughter in goats. Use of more than one product containing neomycin or failure to follow withdrawal times may result in illegal drug residues. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys (growing)

Indication

For the control of mortality associated with E. coli susceptible to neomycin sulfate in growing turkeys.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Goat, No Use Class Stated Or Implied • No use class stated or implied • Cattle, Excluding Veal Calves • Growing • Sheep, No Use Class Stated Or Implied

Composition / specifications

The drug contains 20.3 grams of neomycin sulfate per ounce which is equivalent to 14.2 grams of neomycin base.

Cattle (excluding veal calves)

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Swine

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Sheep

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Goats

Indication

For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days.

Limitations

Add to drinking water or milk. Not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission ofdisease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days before slaughter.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Turkeys (growing)

Indication

For the control of mortality associated with Escherichia coli organisms susceptible to neomycin sulfate in growing turkeys.

Federal Law restricts this drug to use by or on the order of a licensed veterinarian.

Dosage

10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Dog, No Use Class Stated Or Implied • Cat, No Use Class Stated Or Implied

Composition / specifications

Each milliliter of sterile aqueous solution contains 50 milligrams of neomycin sulfate (equivalent to 35 milligrams of neomycin base).

Cats

Indication

Administer to cats for the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.

Dosage

5 milligrams per pound of body weight daily divided into portions administered every 6 to 8 hours for 3 to 5 days. For intramuscular or intravenous use.

Limitations

Dogs

Indication

Administer to dogs for the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.

Dosage

5 milligrams per pound of body weight daily divided into portions administered every 6 to 8 hours for 3 to 5 days. For intramuscular or intravenous use.

Limitations

FDA page: Open in Animal Drugs @ FDA

Species: Dog, No Use Class Stated Or Implied • Cat, No Use Class Stated Or Implied

Composition / specifications

Each gram of the ointment contains 5 milligrams of neomycin sulfate equivalent in activity to 3.5 milligrams of neomycin base.

Dogs

Indication

The drug is intended for use in dogs for the treatment of superficial ocular bacterial infections limited to the conjunctival or the anterior segment of the eye.

Dosage

The drug is applied four times each day.

Limitations

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Cats

Indication

The drug is intended for use in cats for the treatment of superficial ocular bacterial infections limited to the conjunctival or the anterior segment of the eye.

Dosage

The drug is applied four times each day.

Limitations

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Usage

Source: FDA Animal Drugs @ FDA • Reference

Contraindications

Top Reported Reactions (openFDA)

De-duplicated reaction terms grouped by body system from FDA openFDA reports (not verified; does not prove causation).

Digestive

Loss of appetite (1) • Cat Diarrhea (1) • Dog Decreased appetite (1) • Cat

Showing top 5 for Digestive.

Skin & allergy

Ear flapping/twitching (1) • Dog

Showing top 5 for Skin & allergy.

Neurologic

Unsteady walking (1) • Cat Circling - neurological disorder (1) • Dog

Showing top 5 for Neurologic.

Other

Gall bladder inflammation (1) • Cat Found dead (1) • Dog Flaking skin (1) • Cat Elevated total bilirubin (1) • Cat Elevated temperature (1) • Dog

Show more (21)

Elevated serum alkaline phosphatase (1) • Cat Elevated gamma-glutamyl transferase (1) • Cat Elevated alanine aminotransferase (1) • Cat Ear pain (1) • Dog Ear discharge (1) • Dog Dilated pupils (1) • Dog Diabetic ketoacidosis (1) • Cat Dental plaque (1) • Dog Decreased heart rate (1) • Dog Decreased blood urea nitrogen (BUN) or creatinine (1) • Dog Deafness (1) • Cat Dazed (1) • Dog Corneal disorder NOS (1) • Dog Chattering of teeth (1) • Dog Cataract (1) • Dog Bumping into walls (1) • Dog Azotaemia (1) • Cat Anaemia NOS (1) • Dog Abnormal ultrasound finding (1) • Cat Abnormal radiograph finding (1) • Cat Abnormal cytology (1) • Cat

Showing top 5 for Other.

Data source: FDA openFDA Animal & Veterinary adverse event reports.

Adverse Event Case Summaries (openFDA)

These are individual FDA adverse event reports. They are unverified and do not prove the medication caused the reaction.

No case-level openFDA reports are linked for this medication yet.

Data source: FDA openFDA Animal & Veterinary adverse event reports.

Overdose Information

No approved overdose-management text is linked yet. If overdose is suspected, contact a veterinarian or emergency clinic immediately.

Storage & Handling

No approved storage guidance is linked yet for this ingredient. Use manufacturer packaging and veterinary guidance for handling/storage.

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This medication has not been reviewed by a veterinarian yet.

Medical Disclaimer: The medication details provided on Roxee are for informational purposes only and are not a substitute for professional veterinary advice. Always consult your veterinarian about your pet's specific needs.

Neomycin Sulfate

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Neomycin Sulfate

Medication Snapshot

Neomycin Sulfate

Indications / Uses

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Neosol Soluble Powder

Neosol Soluble Powder

Cattle (excluding veal calves)

Swine

Sheep

Goats

Neomix Ag® 325

Neomix Ag® 325 Neomix® 325

Cattle, swine, sheep, and goats, and their offspring

Neomix® 325

Neomix Ag® 325 Neomix® 325

Cattle, swine, sheep, and goats, and their offspring

Neomix® 325 Soluble Powder

Neomix® 325 Soluble Powder Neomix® AG 325 Soluble Powder

Cattle (excluding veal calves or female dairy cattle 20 months of age or older)

Sheep

Swine

Goats

Turkeys (growing)

Neomix® AG 325 Soluble Powder

Neomix® 325 Soluble Powder Neomix® AG 325 Soluble Powder

Cattle (excluding veal calves or female dairy cattle 20 months of age or older)

Sheep

Swine

Goats

Turkeys (growing)

Neomycin Sulfate

Neomycin Sulfate

Cattle (excluding veal calves)

Swine

Sheep

Goats

Neosol-Oral

Neosol-Oral

Cattle (excluding veal calves)

Sheep

Swine

Goats

Turkeys (growing)

NeoMed® Soluble Powder

NeoMed® Soluble Powder

Turkeys (growing)

Sheep

Swine

Goats

Cattle (excluding veal calves)

Neomycin Oral Solution

Neomycin Oral Solution

Cattle (excluding veal calves)