BISMUTH- bismuth subsalicylate suspension 
VEDCO

Disclaimer: 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.

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COMPOSITION:

Bismuth Subsalicylate ... 1.75%

In a palatable aqueous suspension. Flavorings and coloring added.

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 oz. every 2-3 hours

Horses and Cattle- 6 to 10 oz. every 2-3 hours

WARNING:

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

SHAKE WELL BEORE USING.

FOR ORAL USE ONLY

TAKE TIME OBSERVE LABEL DIRECTIONS

STORAGE

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

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

DISTRIBUTED BY

VEDCO, INC

ST. JOSEPH, MO 64504

Package/Label Principal Display Panel

Bottle label

BISMUTH 
bismuth subsalicylate suspension
Product Information
Product TypeOTC ANIMAL DRUGItem 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 Description
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: 03/2013
Document Id: f6069ce8-c4bd-48a9-8fa1-29b90b7ad7d1
Set id: 905a863b-8971-46c1-bc79-5ae7bd9fa904
Version: 1
Effective Time: 20130320
 
VEDCO