Label: 1% IODINE TEAT DIP- iodine solution
-
NDC Code(s):
50748-0017-1,
50748-0017-2,
50748-0017-3,
50748-0017-4, view more50748-0017-5, 50748-0017-6, 50748-0017-7
- Packager: Metz Sales
- 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 June 8, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
INSTRUCTIONS FOR USE
DIRECTIONS:
Immediately after each cow is milked, dip the teats in undiluted METZ IODINE TEAT DIP. Ideally a fresh teat dip solution should be provided for each cow and in no case should the same cup of solution be used for more than 3 or 4 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 3 or 4 days after the last milking. Do not use for cleaning and/or sanitizing milk equipment.
- ACTIVE INGREDIENT
- GENERAL PRECAUTIONS
- KEEP OUT OF REACH OF CHILDREN
-
OTHER SAFETY INFORMATION
FIRST AID
IF SPLASHED IN EYES: Rinse immediately with plenty of water, also under the eyelids, for at least 15 minutes. Get medical attention if irritation occurs.
IN CASE OF CONTACT:Wash off immediately with plenty of water for at least 15 minutes. Get medical attention if symptoms occur.
IF INHALED:Move to fresh air. If symptoms persist, call a physician.
IF SWALLOWED: Drink plenty of water. Do NOT induce vomiting. Never give anything by mouth to an unconscious person. Consult a physician if necessary - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
1% IODINE TEAT DIP
iodine solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50748-0017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 0.004 g in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 0.7886 g in 1 g ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.006 g in 1 g NONOXYNOL-12 (UNII: 6NR43D77O6) 0.059 g in 1 g GLYCERIN (UNII: PDC6A3C0OX) 0.0954 g in 1 g SODIUM HYDROXIDE (UNII: 55X04QC32I) 0.0476 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50748-0017-2 4 in 1 CASE 1 NDC:50748-0017-1 1 g in 1 JUG 2 NDC:50748-0017-3 5 g in 1 PAIL 3 NDC:50748-0017-4 15 g in 1 DRUM 4 NDC:50748-0017-5 30 g in 1 DRUM 5 NDC:50748-0017-6 55 g in 1 DRUM 6 NDC:50748-0017-7 250 g in 1 CONTAINER 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
