Label: SOFT KOTE TEAT DIP- chlorhexidine solution
-
NDC Code(s):
50748-0020-1,
50748-0020-2,
50748-0020-3,
50748-0020-4, view more50748-0020-5, 50748-0020-6, 50748-0020-7
- Packager: Metz Sales
- Category: OTC ANIMAL DRUG LABEL
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 June 8, 2016
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
INSTRUCTIONS FOR USE
USE DIRECTIONS
Immediately after each cow is milked, dip the teats in undiluted METZ SOFT-KOTE TEAT DIP. Ideally a fresh teat dip solution should be provided for each cow and in no case should be the same cup of solution used for more than three or four cows before discarding and providing a fresh solution. Just prior to the next milking, thoroughly wash the treated udder and teats in potable water. Use a fresh towel for each cow and never dip used towels back into the solution. When a cow is being dried off, dip the teats for thee or four days after the last milking. Do not use for cleaning and/or sanitizing milk equipment.
- ACTIVE INGREDIENT
- STORAGE AND HANDLING
- STORAGE AND HANDLING
- KEEP OUT OF REACH OF CHILDREN
- USER SAFETY WARNINGS
-
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, call a 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 symptoms persist, call a physician. - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SOFT KOTE TEAT DIP
chlorhexidine solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50748-0020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE (UNII: R4KO0DY52L) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE 0.025 g in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 0.9317 g in 1 g HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16) 0.003 g in 1 g NONOXYNOL-12 (UNII: 6NR43D77O6) 0.01 g in 1 g GLYCERIN (UNII: PDC6A3C0OX) 0.03 g in 1 g FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.002 g in 1 g ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.001 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50748-0020-2 4 in 1 CASE 1 NDC:50748-0020-1 1 g in 1 JUG 2 NDC:50748-0020-3 5 g in 1 PAIL 3 NDC:50748-0020-4 15 g in 1 DRUM 4 NDC:50748-0020-5 30 g in 1 DRUM 5 NDC:50748-0020-6 55 g in 1 DRUM 6 NDC:50748-0020-7 250 g in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/11/2016 Labeler - Metz Sales (054824487) Establishment Name Address ID/FEI Business Operations Metz Sales 054824487 manufacture, api manufacture