Label: CD 1-2- iodine liquid
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NDC Code(s):
48106-1191-1,
48106-1191-2,
48106-1191-3,
48106-1191-4, view more48106-1191-5, 48106-1191-9
- Packager: BouMatic, LLC
- 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 January 1, 2012
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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INDICATIONS & USAGE
Commercial Grade Iodine Pre-dip
An aid in reducing the spread of mastitis causing organisms.
DIRECTIONS FOR PRE-DIPPING
1. Remove excessive organic soils from udder and teats prior to pre-dipping.
2. Dip or spray cow’s teats thoroughly with CD 1-2.
3. Strip out 3-4 squirts of milk from each quarter.
4. To remove the Iodine Pre-Dip, wipe the teats dry with a single service towel .
5. Attach milking unit.DIRECTIONS FOR POST-DIPPING
Immediately after milking, use CD 1-2 at full strength. Submerge entire teat in CD 1-2.
Allow to air dry. Do not wipe. Always use fresh, full strength CD 1-2. If product in dip cup becomes visibly dirty, discard contents and replenish with CD 1-2 undiluted product.
Do not reuse or return used product to the original container.
If frozen, thaw completely and mix well before using.ACTIVE INGREDIENT: 1% Titratable Iodine
Contains 2% Skin Conditioners
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PRECAUTIONS
DANGER
Keep Out of Reach of Children • Can Cause Eye Damage
Protect eyes when handling. DO NOT get in eyes or on clothing. Harmful if swallowed.
Avoid contamination of food.
FIRST AID
Eyes: In case of contact with eyes, flush immediately with plenty of water for at least 15 minutes. Call a physician.
Internal: If swallowed, promptly rinse mouth then give a large quantity of milk or water. Avoid alchohol. Contact a physician immediately. Never give anything by mouth to an unconscious person.
For Assistance with Medical Emergency, Call 1-800-255-3924.
Refer to Material Safety Data Sheet. - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CD 1-2
iodine liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-1191 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 100 g in 10 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48106-1191-1 3.8 L in 1 DRUM 2 NDC:48106-1191-2 18.9 L in 1 DRUM 3 NDC:48106-1191-3 56.8 L in 1 DRUM 4 NDC:48106-1191-4 114 L in 1 DRUM 5 NDC:48106-1191-5 208 L in 1 DRUM 6 NDC:48106-1191-9 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2007 Labeler - BouMatic, LLC (124727400) Registrant - BouMatic, LLC (124727400) Establishment Name Address ID/FEI Business Operations BouMatic, LLC 124727400 manufacture, api manufacture Establishment Name Address ID/FEI Business Operations BROWN DAIRY EQUIPMENT 017030149 repack Establishment Name Address ID/FEI Business Operations BROWN DAIRY EQUIPMENT 028199899 repack
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