Label: CVS IODINE- iodine, sodium iodide and alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 30, 2022

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  • SPL UNCLASSIFIED SECTION

    CVS Iodine Tincture USP

    Drug Facts

  • Active Ingredient

    Iodine 2%

    Sodium Iodide 2.4%

    Alcohol 47%

  • Purpose

    Antiseptic

  • Indications

    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, 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 reach of children.

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

    • Clean the affected area; apply a small amount on the area 1 to 3 times daily; may be covered with a sterile bandage. If bandaged, let dry first.
  • Inactive Ingredient

    Purified water.

  • Other Information

    Will stain skin and clothing

         

  • PRINCIPAL DISPLAY PANEL

    CVS Iodine Tincture 12-30-22CVS Iodine CVS Health



    Iodine Tincture USP



    First Aid Antiseptic



    1 FL OZ (30 mL)

    capture

  • INGREDIENTS AND APPEARANCE
    CVS IODINE 
    iodine, sodium iodide and alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-213
    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:69842-213-9130 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 not finalpart333A01/01/2008
    Labeler - CVS Pharmacy (062312574)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114manufacture(69842-213) , analysis(69842-213) , pack(69842-213) , label(69842-213)
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