Label: SFP INC. TD-44 SANITIZING TEAT DIP- bronopol liquid
- NDC Code(s): 35723-101-00
- Packager: SUPER FORMULA PRODUCTS INC.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated July 23, 2014
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DIRECTIONS FOR USE:
Immediately after each cow is milked, dip teats in an undiluted solution of SFP Sanitizing TD-44 Teat Dip. Teats should be dipped to the base of the udder. At the end of lactation, the teats should be dipped in SFP Sanitizing TD-44 Teat dip for four days after the last 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.
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. - INGREDIENTS:
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WARNINGS AND PRECAUTIONS
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. - SFP INC. TD-44 SANITIZING TEAT DIP 1041 Liters (35723-101-00)
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INGREDIENTS AND APPEARANCE
SFP INC. TD-44 SANITIZING TEAT DIP
bronopol liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:35723-101 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 LANOLIN (UNII: 7EV65EAW6H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:35723-101-00 1041 L in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/23/2014 Labeler - SUPER FORMULA PRODUCTS INC. (083794508) Establishment Name Address ID/FEI Business Operations Advanced Skin Technologies Inc. 176084556 manufacture, api manufacture
