Label: FORTICEPT UDDER FORTE SANITIZING TEAT DIP- benzethonium chloride, thymol emulsion
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NDC Code(s):
52261-0209-0,
52261-0209-1,
52261-0209-2,
52261-0209-3, view more52261-0209-4, 52261-0209-5
- Packager: Cosco International, 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 September 13, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts Active Ingredient/Purpose
- Inactive Ingredients
- Uses
- Caution
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Directions for use
IMPORTANT: Do not mix FORTICEPTTM UDDER FORTE Teat Dip with water, other teat dips, or any other products. When transferring from this container to any other, make sure that the other container is clean and is the proper container for dipping.
If product in dip cup becomes visibly dirty, discard contents and refill with undiluted product. Do not reuse or return any unused product to the original container.
PRIOR TO MILKING: Wash teats thoroughly right before milking with FORTICEPTTM UDDER WASH solution or pre-milking teat wash to avoid contamination of milk. Teats should be dried with single-service towels. Use proper procedures for udder washing.
POST-MILKING DIPPING: Immediately after each milking, use FORTICEPTTM UDDER FORTE Teat Dip. Submerge each teat full-length into the teat dip cup. Allow to air dry. Do not wipe. Always use fresh, full-strength FORTICEPTTM UDDER FORTE Teat Dip.
- Storage and handling
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FIRST AID
Eye contact: In case of contact, immediately flush eyes with cool running water.
Remove contact lenses and continue flushing with plenty of water for at least 15 minutes. Get medical attention if irritation persists.
Skin contact: Wash the skin with water and soap. Wash clothing before reuse.
Ingestion: DO NOT induce vomiting unless directed to do so by medical personnel.
If large quantities of this material are swallowed, call a poison control center immediately.
- QUESTIONS
- 1Kg
- 3.785Kg
- 5Kg
- 10Kg
- 20Kg
- 1000Kg
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INGREDIENTS AND APPEARANCE
FORTICEPT UDDER FORTE SANITIZING TEAT DIP
benzethonium chloride, thymol emulsionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:52261-0209 Route of Administration Topical Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength benzethonium chloride (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) benzethonium chloride 0.001 kg in 1 kg thymol (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) thymol 0.001 kg in 1 kg Inactive Ingredients Ingredient Name Strength glycerin (UNII: PDC6A3C0OX) 0.04 kg in 1 kg xanthan gum (UNII: TTV12P4NEE) 0.005 kg in 1 kg SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS) 0.006 kg in 1 kg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52261-0209-4 3.785 kg in 1 PAIL 2 NDC:52261-0209-1 20 kg in 1 PAIL 3 NDC:52261-0209-3 5 kg in 1 PAIL 4 NDC:52261-0209-0 1 kg in 1 BOTTLE, PUMP 5 NDC:52261-0209-2 10 kg in 1 PAIL 6 NDC:52261-0209-5 1000 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/29/2016 Labeler - Cosco International, Inc. (016433141) Registrant - Cosco International, Inc. (016433141) Establishment Name Address ID/FEI Business Operations Cosco International, Inc. 016433141 api manufacture, pack, manufacture, label
