Label: CVS DECOLORIZED IODINE- alcohol liquid

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

Drug Label Information

Updated December 18, 2024

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  • SPL UNCLASSIFIED SECTION

    CVS Decolorized Iodine

    Drug Facts

  • Active Ingredient

    Alcohol 48%

  • Purpose

    Antiseptic

  • Uses

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

  • Warnings

    Ask a doctor before use if you have

    deep or puncture wounds. Animal bites. Serious burns. 

    Stop use and consult a doctor if

    Condition persists or gets worse, or if using this product for more than 1 week.

    For external use only. 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 reach of children.

    • In case of accidental ingestion, give milk, then 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 affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.
  • Inactive Ingredient

    Ammonia, iodine, potassium iodide, purified water.

  • Other information

    Will stain skin and clothing

    Flammable

    Keep away from spark, heat and flame

  • PRINCIPAL DISPLAY PANEL

    CVS DecolorizedCVS Decolorized 2022CVSDecolorized.jpg Decolorized



    Iodine



    First Aid Antiseptic



    2 FL OZ (59 mL)

    PRINCIPAL DISPLAY PANEL Decolorized Iodine First Aid Antiseptic 2 FL OZ (59 mL)

  • INGREDIENTS AND APPEARANCE
    CVS DECOLORIZED IODINE 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-207
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.48 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:69842-207-9259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2008
    Labeler - CVS Pharmacy (062312574)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114analysis(69842-207) , manufacture(69842-207) , pack(69842-207) , label(69842-207)
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