Label: DE LA CRUZ DECOLORIZED IODINE- ethyl alcohol liquid

  • NDC Code(s): 24286-1529-8
  • Packager: DLC Laboratories, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients

    Alcohol 45 % denatured with ammonia, Ammonium and Potassium Iodides.

  • Purpose

    Antiseptic

  • Uses

    First aid 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:

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

  • When using this product:

    Do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids. Do not apply over large areas of the body.

  • Keep out of the reach of children.

    In case of acidental ingestion give milk, then give a starch solution made by mixing two tablespoonfools of cornstarch or flour to a pint of water. contact a poison Control Center immediately.

  • Directions

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

  • Inactive Ingredient:

    Purified Water

  • Pther Information:

    Will stain skin and clothing

  • Label

    DLC DecolorizedLabel

  • INGREDIENTS AND APPEARANCE
    DE LA CRUZ DECOLORIZED IODINE 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1529
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.45 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIA (UNII: 5138Q19F1X)  
    IODINE (UNII: 9679TC07X4)  
    POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24286-1529-859 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/06/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/25/1998
    Labeler - DLC Laboratories, Inc. (093351930)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114manufacture(24286-1529) , analysis(24286-1529) , pack(24286-1529) , label(24286-1529)
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