Label: LUGOLS SOLUTION - lugols liquid

  • Category: HUMAN PRESCRIPTION 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 February 1, 2010

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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 Item Code (Source) NDC:10481-0111
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 0.4 g  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
    WATER (UNII: 059QF0KO0R)  
    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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