Label: METZ 0.5% FRESH TEAT DIP- iodine solution
- NDC Code(s): 86067-0021-1, 86067-0021-2
- Packager: Surpass Chemical Company, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 27, 2022
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- DESCRIPTION
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INSTRUCTIONS FOR USE
DIRECTIONS:
PRE-MILKING: Throughly clean all teats. If water or sanitizer is used to clean the teats, be sure to completely dry the teats with a single service paper towel. Forestrip two or three streams Dip the cow's teats full length with Metz Fresh 0.5% Teat Dip. Wait 15-30 seconds. Remove all residues by throughly drying the teats with a clean, single service paper towel. Attach milker unit.
POST-MILKING: Immediately after milking, dip all teats to the base of the udder with Metz Fresh 0.5% Teat Dip. On dry cows, dip each teat once per day for five days following the last milking.
GENERAL: Use teat dipping cups made of plastic, rubber, or stainless steel. Do not use cups made of aluminum. - GENERAL PRECAUTIONS
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PRECAUTIONS
PRECAUTIONARY STATEMENTS
Prevention: Do not breathe dust/fume/gas/mist/vapors/spray Wash face, hands and any exposed skin thoroughly after
handling Do not eat, drink or smoke when using this product
Response: Get medical advice/attention if you feel unwell
Disposal: Dispose of contents/container to an approved waste disposal plant -
OTHER SAFETY INFORMATION
FIRST AID:
IF SPLASHED IN EYES:Rinse thoroughly with plenty of water, also under the eyelids. If symptoms persist, call a physician.
IN CASE OF CONTACT: Wash with soap and water.
IF INHALED: Remove to fresh air.
IF SWALLOWED: Rinse mouth immediately and drink plenty of water. Never give anything by mouth to an unconscious person. - ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
METZ 0.5% FRESH TEAT DIP
iodine solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86067-0021 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 0.0275 g in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 0.8787 g in 1 g C9-11 PARETH-8 (UNII: 80E6PSE1XL) 0.0354 g in 1 g GLYCERIN (UNII: PDC6A3C0OX) 0.05 g in 1 g LAURETH-11 CARBOXYLIC ACID (UNII: CK7N38KKFK) 0.0033 g in 1 g SODIUM HYDROXIDE (UNII: 55X04QC32I) 0.0021 g in 1 g ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.003 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86067-0021-1 128 g in 1 DRUM 2 NDC:86067-0021-2 470 g in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/10/2016 Labeler - Surpass Chemical Company, Inc. (002075133) Establishment Name Address ID/FEI Business Operations Surpass Chemical Company, Inc. 002075133 manufacture, api manufacture