Label: IODINE TINCTURE WHITE- iodine tincture solution/ drops

  • NDC Code(s): 70242-109-01
  • Packager: Dannso Corp./d.b.a. Essential Products
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2023

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  • Active ingredients

    Iodine 2%

  • Purpose

    First aid antiseptic

  • Use

    First aid to help prevent sking infection in

    • minor cuts
    • scrapes
    • burns
  • WARNINGS

    Warnings

    For external use only. Avoid contact with eyes or with mucous membrane. Keep out of the reach of children. Children under 2 years please consult a physician. Do not apply on irritated skin, in or near eyes or mocuos memebranes, on wounds or damamged skin, or if it causes allergic reaction. In case of accidental ingestion, seek professional assistance or contact Poison Control Center immedialately.


  • Inactive Ingredient

    Ammonium, Deionized Water, Isopropyl Alcohol, Sodium Iodine.

  • Stop use and ask a doctor

    If condition persists or gets worse

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    • Clean the affected area and dry thorougkyapply.
    • Apply a thin layer 1 to 3 times daily
    • May be covered with a sterile bandage
  • Questions or Comments?

    Distributed by

    Essential Products Miami FL 33126

    www.essentialproductsuse.com

    Made in U.S.A.

  • Principal display panel

    IODO BLANCO

    Label

  • INGREDIENTS AND APPEARANCE
    IODINE TINCTURE WHITE 
    iodine tincture solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70242-109
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIUM SALICYLATE (UNII: 0T3Q181657)  
    Isopropyl Alcohol (UNII: ND2M416302)  
    Sodium Iodide (UNII: F5WR8N145C)  
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70242-109-0130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/08/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00508/08/2015
    Labeler - Dannso Corp./d.b.a. Essential Products (059741071)
    Registrant - Dannso Corp./d.b.a. Essential Products (059741071)
    Establishment
    NameAddressID/FEIBusiness Operations
    World Perfume, Inc101312044MANUFACTURE(70242-109)
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