Label: METS SOFT KOTE TEAT SPRA- chlorhexidine solution
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NDC Code(s):
86067-0028-1,
86067-0028-2,
86067-0028-3,
86067-0028-4, view more86067-0028-5
- Packager: Surpass Chemical. Company, 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 May 15, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- DESCRIPTION
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INSTRUCTIONS FOR USE
DIRECTIONS:
Immediately after each milking dip each teat in undiluted North Country Dairy Supply METZ Soft Kote Spray. Teats should be dipped to the base of the udder. If the dip becomes visibly dirty or contains sediment, replace with fresh solution.
At the end of lactation, the teat should be dipped with North Country Dairy Supply METZ Soft Kote Spray for four days after the last milking.
Teat should be thoroughly washed and dried before milking using a North Country Dairy Supply Predip and individual towels. - OTHER SAFETY INFORMATION
- ACTIVE INGREDIENT
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OTHER SAFETY INFORMATION
FIRST AID:
IF SPLASHED IN EYES:Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
IN CASE OF CONTACT:Wash skin with soap and water. Remove and wash contaminated clothing before re-use. If skin irritation persists, cal la physician.
IF INHALED:Move to fresh air.
IF SWALLOWED:Drink plenty of water. Do not induce vomiting without medical advice. Never give anything by mouth to an unconscious person. If symptons persist, call a physician. - SAFE HANDLING WARNING
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
METS SOFT KOTE TEAT SPRA
chlorhexidine solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86067-0028 Route of Administration Topical Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE (UNII: R4KO0DY52L) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE 0.025 kg in 1 kg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 0.9347 kg in 1 kg C9-11 PARETH-8 (UNII: 80E6PSE1XL) 0.01 kg in 1 kg GLYCERIN (UNII: PDC6A3C0OX) 0.03 kg in 1 kg FD&C BLUE NO. 2 (UNII: L06K8R7DQK) 0.0002 kg in 1 kg ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.0001 kg in 1 kg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86067-0028-1 19.05 kg in 1 PAIL 2 NDC:86067-0028-2 57.15 kg in 1 DRUM 3 NDC:86067-0028-3 114.76 kg in 1 DRUM 4 NDC:86067-0028-4 210.01 kg in 1 DRUM 5 NDC:86067-0028-5 1222.43 kg in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/17/2019 Labeler - Surpass Chemical. Company, Inc. (002075133) Establishment Name Address ID/FEI Business Operations Surpass Chemical. Company, Inc. 002075133 manufacture, api manufacture
