CORRECTIVE- bismuth subsalicylate suspension

Corrective by

Drug Labeling and Warnings

Corrective by is a Animal medication manufactured, distributed, or labeled by Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NDC:

57319-393-09Corrective SuspensionAnti-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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CORRECTIVE 
bismuth subsalicylate suspension

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 57319-393
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE)	BISMUTH SUBSALICYLATE	18 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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
Shape		Size
Flavor	WINTERGREEN	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57319-393-09	3785 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		04/20/2000

Labeler - Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc. (150711039)