Label: LUGOLS SOLUTION - iodine liquid

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 02/10

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  • DESCRIPTION

    Strong Iodine Solution USP a topical anti-infective agent.

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  • HOW SUPPLIED


    Applied with a q-tip.

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  • SPL UNCLASSIFIED SECTION

    May be stored at room temperature.

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  • WARNINGS AND PRECAUTIONS

    Single use only. Do not reuse.  Discard after one  use. Do not use if  seal is broken. Restricted to use by or on the order of a licensed Physician. Keep cap tightly sealed and product from light.



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  • INGREDIENTS AND APPEARANCE
    LUGOLS SOLUTION 
    lugols liquid
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:10481-0111
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IODINE (IODINE) IODINE 0.4 g  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    POTASSIUM IODIDE  
    WATER  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10481-0111-8 8 g in 1 BOTTLE, GLASS
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 02/01/2010
    Labeler - Gordon Laboratories (002333847)
    Registrant - Gordon Laboratories (002333847)
    Establishment
    Name Address ID/FEI Business Operations
    Gordon Laboratories 002333847 manufacture
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