Label: CVS POVIDONE-IODINE- povidone iodine liquid

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

Drug Label Information

Updated December 20, 2023

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  • SPL UNCLASSIFIED SECTION

    CVS Povidone-Iodine

    Drug Facts

  • Active Ingredient

    Povidone-Iodine 10% (1% Available iodine)

  • Purpose

    First Aid Antiseptic

  • Uses

    First aid to help prevent infection in in minor: cuts, scrapes and burns.

  • Warnings

    For external use only

    Do not use

    in the eyes. Over large areas of the body.

    Ask a doctor before use

    in case of deep or puncture wounds, animal bites, or serious burns. 

    Stop use and consult a doctor if:

    The condition persists or gets worse. Need to use this product for more than 1 week.

    Keep out of reach of children.

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

    Citric acid, Dibasic sodium Phosphate, Glycerin, Nonoxynol-9, Purified water, sodium hydroxide.

  • PRINCIPAL DISPLAY PANEL

    CVSPov.jpgCVS Health

    Povidone-

    Iodine

    8 FL OZ (237 mL)

    CVS Health Povidone- Iodine 8 FL OZ (237 mL)

  • INGREDIENTS AND APPEARANCE
    CVS POVIDONE-IODINE 
    povidone iodine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-325
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-325-98237 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(69842-325) , manufacture(69842-325) , pack(69842-325) , label(69842-325)
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