Label: LUGOLS SOLUTION- lugols liquid

  • Category: HUMAN PRESCRIPTION DRUG LABEL

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.

  • HOW SUPPLIED


    Applied with a q-tip.

  • SPL UNCLASSIFIED SECTION

    May be stored at room temperature.

  • 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.



  • PRINCIPAL DISPLAY PANEL

    Image of Lugols Labels

  • INGREDIENTS AND APPEARANCE
    LUGOLS SOLUTION 
    lugols liquid
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:10481-0111
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE0.4 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10481-0111-88 g in 1 BOTTLE, GLASS
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/01/2010
    Labeler - Gordon Laboratories (002333847)
    Registrant - Gordon Laboratories (002333847)
    Establishment
    NameAddressID/FEIBusiness Operations
    Gordon Laboratories002333847manufacture
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