Label: GNP IDOINDE TINCTURE 2% MILD- iodine and sodium iodide and alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 14, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug facts

  • Active Ingredients

    Iodine 2%

    Sodium iodide 2.4%

    Alcohol 47%

  • Purpose

    Antiseptic

  • Uses:

    To help prevent infection in minor cuts, scrapes and burns.

  • Warnings:

    For external use only

  • Ask a doctor before use if you have

    • deep or puncture wounds.
    • animal bites.
    • serious burns.
  • Stop use and ask a doctor if

    condition persists or gets worse, or if using this product for longer than 1 week.

  • When using this product.

    Do not use in eyes. If contact occurs, flush with large amounts of water while lifting upper and lower eyelids.

    Do not apply over large areas of the body.

  • Keep out of reach ofchildren

    In case of accidental ingestion, give milk then give a starch solution made by mixing two tablespoonfuls of cornstarch or flour to a pint of water. Contact a Poison Control Center immediately.

  • Directions:

    Clean the affected area. Apply a small amount to the affeted area 1 to 3 times daily. May be covered with sterile bandage. If bandaged, let dry first.

  • Inactive ingredient:

    Purified Water.

  • Other information:

    Will stain skin and clothing

    Dist. by: AmerisourceBergen

    1300 Morris Dr., Chesterbrook, PA 19087

  • Questions or Comments?

    1-800-662-3435     www.goodneighborpharmacy.com

  • Principal Display Panel

    label

    Good Neighbor Pharmacy   NDC 24385-0213-10

    Iodine Tincture USP 2% Mild

    Antiseptic First Aid

    First Aid Antiseptic

    Alcohol 47%

    FLAMMABLE: Keep away from sparks, heal & flame.

    1 FL OZ (30 mL)

  • INGREDIENTS AND APPEARANCE
    GNP IDOINDE TINCTURE 2% MILD 
    iodine and sodium iodide and alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-213
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE20 mg  in 1 mL
    SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION20.4 mg  in 1 mL
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL470 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24385-213-1030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/16/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2008
    Labeler - Amerisource Bergen (007914906)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114manufacture(24385-213) , analysis(24385-213) , pack(24385-213) , label(24385-213)
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