Label: AL LABORATORIES IODINE UDDER WASH - iodine liquid

  • NDC Code(s): 50138-267-01, 50138-267-02, 50138-267-03, 50138-267-04, view more
    50138-267-05, 50138-267-06, 50138-267-07, 50138-267-08
  • Packager: EXL Laboratories, LLC
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 11/12

If you are a consumer or patient please visit this version.

  • Usage Directions Active Ingredients

    DIRECTIONS FOR USE:

    1. Prepare the udder wash solution in a plastic pail, using 1 oz. (30 ml) of this product per 5 gallons (20L) of lukewarm water (110 - 115 degrees F, 43-46 degrees C). This will give an udder wash solution containing 25ppm of iodine.

    2. Approximately one minute before applying the milking unit, wash and massage teats with a clean towel wetted with the udder wash solution. Use a second towel to dry the teats before applying the milking unit.

    3. Discard the used towels. Do not reuse towels or dip used towels back into the udder wash solution.

    DO NOT USE THIS PRODUCT FOR CLEANING AND/OR SANITIZING EQUIPMENT

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  • Warnings First Aid Storage and Disposal

    DANGER!

    KEEP OUT OF THE REACH OF CHILDREN.

    CAUSES SEVERE EYE AND SKIN IRRITATIONS OR BURNS.

    MAY CAUSE DEATH IF SWALLOWED - HARMFUL IF INHALED.

    CONTAINS PHOSPHORIC ACID AND IODINE-SURFACTANT COMPLEX.

    SEE BELOW FOR ADDITIONAL PRECAUTIONS AND/OR CONSULT MATERIAL SAFETY DATA SHEET.

    PRECAUTIONS: Protect eyes. skin and clothing from contact with product. When handling, wear chemical goggles, rubber boots, rubber apron and rubber gloves to prevent injury. Keep container tightly closed when not in use. Use with adequate ventilation. Wash thoroughly after handling product.

    TOLL-FREE EMERGENCY NUMBER: 1-800-424-9300

    FIRST AID:

    EXTERNAL: In case of contact, immediately flush contaminated skin with plenty of water for at least 15 minutes. Remove contaminated clothing and shoes while flushing with water. If irritation occurs or burn occurs, call a physician.

    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. Call a physician.

    INHALATION: Remove to fresh air. Get medical attention.

    STORAGE AND DISPOSAL:

    Store this product in a cool, dry area away from direct sunlight and heat to avoid deterioration. Store in a locked cabinet or room to keep out of the reach of children. Dispose of only in compliance with federal, state and local laws.

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  • Product Label

    A and L Laboratories

    IODINE UDDER WASH

    Part #

    267

    UDDER WASH

    CORROSIVE  8

    Net Contents: 15 GALLONS (56.8 L)

    Lot # 00010252A  

    Expires: 10/2014

    EXL Laboratories, LLC

    1001 Glenwood Ave.

    Minneapolis, MN 55405

    CORROSIVE LIQUIDS, N. O. S.

    (PHOSPHORIC ACID), 8, UN1760, PG II

    Exl Lab Iodine Udder2 Label

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  • INGREDIENTS AND APPEARANCE
    AL LABORATORIES IODINE UDDER WASH 
    iodine liquid
    Product Information
    Product Type OTC ANIMAL DRUG LABEL Item Code (Source) NDC:50138-267
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IODINE (IODINE) IODINE 25 mg  in 1 L
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:50138-267-01 9.5 L in 1 JUG
    2 NDC:50138-267-02 19 L in 1 JUG
    3 NDC:50138-267-03 56.8 L in 1 DRUM
    4 NDC:50138-267-04 114 L in 1 DRUM
    5 NDC:50138-267-05 208 L in 1 DRUM
    6 NDC:50138-267-06 946 L in 1 DRUM
    7 NDC:50138-267-07 1003 L in 1 DRUM
    8 NDC:50138-267-08 1041 L in 1 DRUM
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 05/01/2005
    Labeler - EXL Laboratories, LLC (927483458)
    Registrant - EXL Laboratories, LLC (927483458)
    Establishment
    Name Address ID/FEI Business Operations
    EXL Laboratories, LLC 927483458 api manufacture, manufacture
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