Label: NORTH COUNTRY DAIRY SUPPLY TD7003BK- iodine solution
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NDC Code(s):
86067-0007-1,
86067-0007-2,
86067-0007-3,
86067-0007-4, view more86067-0007-5, 86067-0007-6, 86067-0007-7
- 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 18, 2016
If you are a consumer or patient please visit this version.
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- GENERAL PRECAUTIONS
- KEEP OUT OF REACH OF CHILDREN
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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 skin with soap and water. If symptoms persist, call a physician.
IF INHALED: Move to fresh air. If symptoms persist, call a physician.
IF SWALLOWED: Drink plenty of water. Do NOT induce vomiting. Consult a physician if necessary. -
INSTRUCTIONS FOR USE
DIRECTIONS:
Teat Dip 7003BK is an effective Chlorhexidine teat dip. It is useful as an aid in controlling the spread of organisms that may cause mastitis, when part of a total dairy hygiene program.
Teat Dip 7003BK is designed to use full strength - no messy mixing and measuring needed. Immediately after removing inflation, immerse each teat in Teat Dip 7003BK, full strength. Allow to air dry. Do not wipe.- Before milking, first wash cow’s udders and teats with warm water to remove gross soil.
- Wash udder using 1 oz. of North Country udder wash to 4 gallons tepid water. A single use paper towel should be used to wash each cow separately. Wash and massage teats and udder. Wipe off excess. Discard towel.
- Use a strip cup to check milk from each quarter before attaching inflation.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NORTH COUNTRY DAIRY SUPPLY TD7003BK
iodine solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86067-0007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE (UNII: R4KO0DY52L) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE 0.0278 kg in 1 kg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 0.92451 kg in 1 kg POLYSORBATE 80 (UNII: 6OZP39ZG8H) 0.00509 kg in 1 kg GLYCERIN (UNII: PDC6A3C0OX) 0.03865 kg in 1 kg ISOPROPYL ALCOHOL (UNII: ND2M416302) 0.00271 kg in 1 kg ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.00002 kg in 1 kg HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP) 0.00122 kg in 1 kg METHYLENE BLUE (UNII: T42P99266K) 0.00004 kg in 1 kg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86067-0007-2 4 in 1 CASE 1 NDC:86067-0007-1 3.81 kg in 1 NOT APPLICABLE 2 NDC:86067-0007-3 19.05 kg in 1 PAIL 3 NDC:86067-0007-4 57.1499 kg in 1 DRUM 4 NDC:86067-0007-5 114.2998 kg in 1 DRUM 5 NDC:86067-0007-6 209.5497 kg in 1 DRUM 6 NDC:86067-0007-7 1142.9983 kg in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/18/2016 Labeler - Surpass Chemical Company, Inc. (002075133) Establishment Name Address ID/FEI Business Operations Surpass Chemical Company, Inc. 002075133 manufacture, api manufacture
