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BISMUTH (bismuth subsalicylate) suspension
[VEDCO]


Category DEA Schedule Marketing Status
OTC ANIMAL DRUG LABEL unapproved drug other
NOTE:THIS DRUG HAS NOT BEEN FOUND BY FDA TO BE SAFE AND EFFECTIVE, AND THIS LABELING HAS NOT BEEN APPROVED BY FDA. For further information about unapproved drugs, click here.
Drug Label Sections

NDC 50989-527-29
BISMU-KOTE
ANTI-DIARRHEAL LIQUID
PALATABLE ORAL SUSPENSION

NET CONTENTS: 1 GALLON (3.785 L)

VEDCO

KEEP OUT OF REACH OF CHILDREN

FOR ANIMAL USE ONLY

INDICATIONS:

A palatable oral suspension for use as an aid in controlling simple diarrhea in cattle, horses, dogs and cats.

CAUTION:

This product contains salicylate; do not administer with other salicylate-containing products, such as aspirin. 

DOSAGE AND ADMINISTRATION:

Administer orally

Dogs and Cats- 1 to 3 tablespoonfuls every 1-3 hours

Calves and Foals- 3 to 4 ounces every 2-3 hours

Horses and Cattle- 6 to 10 ounces every 2-3 hours

WARNING:

If diarrhea persists after using this product for 2 days, contact a veterinarian.

Rev 12-98

Distributed By

VEDCO, INC.

St. Joseph, MO 64504

COMPOSITION:

Bismuth Subsalicylate............1.75%

In a palatable aqueous suspension.

Flavoring and coloring added.

SHAKE WELL BEFORE USING.

FOR ORAL USE ONLY

KEEP FROM FREEZING.

Store at room temperature above 37ºC (98.6ºF). 

TAKE TIME OBSERVE LABEL DIRECTIONS

´╗┐Lot No.:

Exp. Date:

Package/Label Principal Display Panel

Bottle label

BISMUTH 
bismuth subsalicylate suspension
Product Information
Product TypeOTC ANIMAL DRUG LABELItem Code (Source)NDC:50989-527
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISMUTH SUBSALICYLATE (BISMUTH CATION) BISMUTH SUBSALICYLATE18 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GUAR GUM 
POTASSIUM SORBATE 
SACCHARIN SODIUM 
METHYL SALICYLATE 
WATER 
D&C RED NO. 33 
SILICON DIOXIDE 
Product Characteristics
ColorpinkScore    
ShapeSize
FlavorWINTERGREENImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50989-527-293785 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other03/27/2000
Labeler - VEDCO (021634266)

Revised: 9/2013
 
VEDCO

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