AST INC. PRO-4 BARRIER TEAT DIP- bronopol solution

AST Inc. PRO-4 BARRIER TEAT DIP by

Drug Labeling and Warnings

AST Inc. PRO-4 BARRIER TEAT DIP by is a Animal medication manufactured, distributed, or labeled by Advanced Skin Technologies Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DANGER:

Keep Out of Reach of Children

Can Cause Eye Damage

Protect eyes when handling. DO NOT get in eyes or on clothing, Harmful if swallowed. Avoid contamination of food.

FIRST AID:

Eyes: In case of contact with eyes, flush immediately with plenty of water for at least 15 minutes. Call a physician..

Internal: DO NOT TAKE INTERNALLY. If swallowed, drink large quantities of water, and call a physician immediately.

CAUTION : AVOID FREEZING--

If frozen, let thaw and shake thoroughly before using.

INGREDIENTS:

Active Ingredient - 2 Bromo, 2 Nitro-propanediol 0.245

Also contains-Lanolin and Barrier System and glycerin, Phenoxyethanol - 1% used as preservative

DIRECTIONS FOR USE:

Immediately after each cow is milked, dip teats in an undiluted solution of AST Barrier Teat Dip. Teats should be dipped to the base of the udder. At the end of lactation, teats should be dipped in AST Pro-4 Barrier Teat Dip for 4 days after milking. Teats and udders should be thoroughly washed and dried before milking*, using potable water and individual paper towels to prevent contamination of milk. Blot dry. If the dip becomes visibly dirty or contains sediment, use a fresh solution.

(*with AST Udder Wash or similar)

SPL UNCLASSIFIED SECTION

Teats should be thoroughly washed and dried before milking, using potable water, a suitable cleanser* and individual paper towels to remove soil and to prevent contamination of milk.

Package Labeling:

INGREDIENTS AND APPEARANCE

AST INC. PRO-4 BARRIER TEAT DIP 
bronopol solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 52657-0103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BRONOPOL (UNII: 6PU1E16C9W) (BRONOPOL - UNII:6PU1E16C9W)	BRONOPOL	2.45 mg  in 0.001 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
LANOLIN (UNII: 7EV65EAW6H)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52657-0103-0	56.7811768 L in 1 JUG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/18/2022

Labeler - Advanced Skin Technologies Inc. (176084556)

Establishment
Name	Address	ID/FEI	Business Operations
Advanced Skin Technologies Inc.		176084556	manufacture, api manufacture