Label: AL LABORATORIES 10 MIX PLUS - iodine liquid
view more50138-440-05, 50138-440-06, 50138-440-07, 50138-440-08
- Packager: EXL Laboratories, 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.
Updated January 24, 2013
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- Usage Directions Active Ingredient
DO NOT USE AS IS. WHEN MIXING WITH WATER ALWAYS USE A CONTAINER THAT IS FREE OF RESIDUE.
- 1% Iodine Teat Dip with 10% Conditioners. Mix 1 part product with 2 parts potable water.
- 0.5% Iodine Teat Dip with 5% Conditioners. Mix 1 part product with 5 parts potable water.
- 0.25% Iodine Teat Dip with 2.5% Conditioners. Mix 1 part product with 11 parts potable water.
PRE-DIPPING/SPRAYING: Teats should be clean and dry before dipping. Dip/spray with undiluted product and allow 30-60 seconds contact time. Wipe the teats dry.
POST-DIPPING/SPRAYING: Dip/spray teats with undiluted product after milking. Allow to air dry. With freshening cows, begin dipping teats twice daily for about 10 days before calving. For dry cows, dip spray teats once a day for 3-4 days following the last milking. DURING COLD WEATHER do not turn out cows until teats are dry.
UDDER WASH: Cow’s teats should be washed just prior to milking, using ready-to-use product at one of the following dilutions: 0.25% iodine = 2oz/gal
(60ml/4L): 0.5% iodine = 1oz/gal (30ml/4L): 1% iodine = 1oz/2gal (30ml/8L)
DO NOT USE THIS PRODUCT FOR CLEANING AND/OR SANITIZING EQUIPMENT
IMPORTANT: TEAT IRRITATION OR CHAPPING: Teat dips have the potential to cause irritation or chapping. If you observe abnormal irritation or chapping, call 1-800-225-3832 or contact your dealer.
ACTIVE INGREDIENTS: Nonylphenolyethoxy (12 moles EO) ethanol-iodine complex providing 3% titratable iodine (30,000 ppm)
Contains 30% skin conditioners.Close
- Caution First Aid Storage and Disposal
KEEP OUT OF REACH OF CHILDREN
HARMFUL IF SWALLOWED – HARMFUL IF INHALED – CAUSES EYE IRRITATION
SEE BELOW FOR ADDITIONAL PRECAUTIONS OR CONSULT MSDS SHEET
TOLL FREE EMERGENCY NUMBER: 1-800-424-9300
PRECAUTIONS: Protect eyes from contact with this product. Keep container tightly closed when not in use. Use with adequate ventilation. Wash thoroughly after handling product.
EXTERNAL: In case of contact, immediately flush contaminated skin with plenty of water. If irritation occurs and persists call a physician.
INTERNAL: If conscious, dilute by giving several glasses of water or milk. Do not induct vomiting. If vomiting does occur, repeat giving several glasses of water or milk. Give prompt medical attention. NEVER GIVE ANYTHING BY MOUTH TO AN UNCONSCIOUS PERSON.
EYES: Immediately flush with plenty of clean running water for at least 15 minutes holding eyelids apart to ensure flushing of the entire eye surface. If irritation persists, call a physician.
STORAGE AND DISPOSAL: Store this product in a cold, dry area away from direct sunlight and heat to avoid deterioration. Store in a locked cabinet or room to keep it out of the reach of children. Dispose of according to Federal, State, and local laws.
SPILLAGE: In case of small spill (less than one gallon), flood area with large quantity of water. For larger spills, contain and remove with inert absorbent and dispose of according to Federal, State, and local laws.
KEEP FROM FREEZING
- Product Label
A and L Laboratories
10 MIX PLUS ™
IODINE TEAT DIP CONCENTRATE
Manufactured by: EXL Laboratories, LLC. 1001 Glenwood Ave. Minneapolis, MN 55405
Net Contents: 15 GALLONS (56.8L)
Lot #: 00011022A Expires: 11/2014
Part #: 822440
- INGREDIENTS AND APPEARANCE
AL LABORATORIES 10 MIX PLUS
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50138-440 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 30000 mg in 1 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50138-440-01 9.5 L in 1 JUG 2 NDC:50138-440-02 19 L in 1 JUG 3 NDC:50138-440-03 56.8 L in 1 DRUM 4 NDC:50138-440-04 114 L in 1 DRUM 5 NDC:50138-440-05 208 L in 1 DRUM 6 NDC:50138-440-06 946 L in 1 DRUM 7 NDC:50138-440-07 1003 L in 1 DRUM 8 NDC:50138-440-08 1041 L in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/01/2000 Labeler - EXL Laboratories, LLC (927483458) Registrant - EXL Laboratories, LLC (927483458) Establishment Name Address ID/FEI Business Operations EXL Laboratories, LLC 927483458 api manufacture, manufacture