Label: SODIUM IODIDE-IODINE COMPLEX - iodine concentrate 

  • Label RSS
  • 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 05/14

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  • WARNINGS

    ! DANGER

    Causes severe eye, skin, and digestive tract burns

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  • SPL UNCLASSIFIED SECTION

    FIRST AID
    Eyes:
      Immediately flush with plenty of water at least 15 minutes.  If easy to do, remove contact lenses while flushing.  Get medical attention immediately.

    Skin:  Immediately flush with plenty of water at least 15 minutes while removing contaminated clothing.  Get medical attention immediately.

    If swallowed:   DO NOT induce vomiting.  Get medical attention immediately.  If victim is fully conscious, give a cupful of water.  Never give anything my mouth to an unconscious person.

    For additional information, consult the Material Safety Data Sheet (MSDS).

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  • SPL UNCLASSIFIED SECTION

    DeLaval Manufacturing
    11100 N. Congress Ave.
    Kansas City, MO 64153
    816-891-7700
    (M-F, 8:00-4:00 Central Time)

    0575-D1109

    NET CONTENTS:

    LOT NO.:

    EXP DATE:

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  • SPL UNCLASSIFIED SECTION

    DOT DESCRIPTION
    UN1760, Corrosive Liquid,
    N.O.S. contains Iodine
    Complex), 8, PG II

    0575

    CORROSIVE  8

    CHEMTREC EMERGENCY NO.
    1-800-424-9300

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  • INGREDIENTS AND APPEARANCE
    SODIUM IODIDE-IODINE COMPLEX 
    iodine concentrate
    Product Information
    Product Type OTC ANIMAL DRUG LABEL Item Code (Source) NDC:33392-575
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Iodine (Iodine) Iodine 1.37 kg  in 1 L
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:33392-575-99 99.3 L in 1 DRUM
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 01/01/2012
    Labeler - WestAgro, Inc. (069288728)
    Registrant - WestAgro, Inc. (069288728)
    Establishment
    Name Address ID/FEI Business Operations
    WestAgro, Inc. 147528723 analysis, label, manufacture, pack, api manufacture
    Establishment
    Name Address ID/FEI Business Operations
    K Klean dba WestAgro, Inc. 002222368 analysis, label, manufacture, pack, api manufacture
    Establishment
    Name Address ID/FEI Business Operations
    WestAgro, Inc. 044610140 analysis, label, manufacture, pack, api manufacture
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