Label: LUGOLS SOLUTION- iodine solution

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

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Drug Label Information

Updated November 6, 2019

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  • BOXED WARNING (What is this?)

    Single Use Only. CAUTION: Restricted to use by or on the order of a physcian. Do not use if seal has been broken.

    Lugol

  • PRINCIPAL DISPLAY PANEL

    Lugols

  • INGREDIENTS AND APPEARANCE
    LUGOLS SOLUTION 
    iodine solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70804-005
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE1 g  in 5 g
    Product Characteristics
    ColorblackScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70804-005-081 g in 1 VIAL; Type 0: Not a Combination Product01/27/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/27/2017
    Labeler - PURTEX INC (004390834)
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Safety

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