CORRECTIVE- bismuth subsalicylate suspension 
Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.

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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Corrective Suspension
Anti-Diarrheal Suspension

NDC 57319-393-09
Corrective Suspension
Anti-Diarrheal Suspension  

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

Net Contents:

3.785L (1 Gal.)

Manufactured For:

PHOENIX

PHARMACEUTICAL, INC.

St. Joseph, MO 64503

INDICATIONS:

For oral administration as an aid in the treatment of noninfectious diarrhea in horses, cattle, dogs and cats.

DOSAGE:

Cattle 6 - 10 oz. Every 2 - 3 hours
Calves 3 - 4 oz. Every 2 - 3 hours
Horses 6 - 10 oz. Every 2 - 3 hours
Foals 3 - 4 oz. Every 2 - 3 hours
Dogs 1 - 3 Tbls. (1/2 - 2 oz.) Every 1 - 3 hours
Cats 1 - 3 Tbls. (1/2 - 2 oz.) Every 1 - 3 hours

WARNING:

If symptoms persist after using this product for 2 to 3 days consult a veterinarian.

FOR ANIMAL USE ONLY

NOT FOR HUMAN USE

Rev 11-01

Lot No.

Exp. Date

CONTAINS:

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

Administration: Oral.

SHAKE WELL BEFORE USING.
KEEP FROM FREEZING.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN

TAKE TIME OBSERVE LABEL DIRECTIONS

Manufactured by:
Ameri-Pac
St. Joseph, MO 64502

Bottle Label

CORRECTIVE 
bismuth subsalicylate suspension
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57319-393
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE18 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GUAR GUM (UNII: E89I1637KE)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Product Characteristics
Color    Score    
ShapeSize
FlavorWINTERGREENImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57319-393-093785 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other04/20/2000
Labeler - Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc. (150711039)

Revised: 9/2013
Document Id: f4ffcc49-6092-4d02-b831-4b004ec6fc7c
Set id: 3d1c67bf-21ef-44f9-b0b3-2e8be0c5fd7d
Version: 2
Effective Time: 20130917
 
Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.