Animal NDC 57319-393-09 Corrective

Bismuth Subsalicylate

Animal Product Information

Field Name Field Value
Animal NDC Code 57319-393-09
Proprietary Name Corrective What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Bismuth Subsalicylate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Labeler Name Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.
Product Type Otc Animal Drug
Usage Information
    For oral administration as an aid in the treatment of noninfectious diarrhea in horses, cattle, dogs and cats.
Active Ingredient(s)
  • Bismuth Subsalicylate
Inactive Ingredient(s)
  • WATER (059QF0KO0R)
  • GUAR GUM (E89I1637KE)
  • METHYL SALICYLATE (LAV5U5022Y)
  • POTASSIUM SORBATE (1VPU26JZZ4)
  • SACCHARIN SODIUM (SB8ZUX40TY)
  • D&C RED NO. 33 (9DBA0SBB0L)
  • SILICON DIOXIDE (ETJ7Z6XBU4)
  • WATER (059QF0KO0R)
  • GUAR GUM (E89I1637KE)
  • METHYL SALICYLATE (LAV5U5022Y)
  • POTASSIUM SORBATE (1VPU26JZZ4)
  • SACCHARIN SODIUM (SB8ZUX40TY)
  • D&C RED NO. 33 (9DBA0SBB0L)
  • SILICON DIOXIDE (ETJ7Z6XBU4)
Marketing Category UNAPPROVED DRUG OTHER What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Corrective Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



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.


Keep This And All Medications Out Of The Reach Of Children



TAKE TIME OBSERVE LABEL DIRECTIONS

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


* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.