Label: POVIDONE-LODINE PREP PAD patch

  • NDC Code(s): 84449-002-01
  • Packager: SHENZHEN BENLIJU BIO-TECH CO.,LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 19, 2024

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  • ACTIVE INGREDIENT

    Available Iodine

  • PURPOSE

    disinfect

  • INDICATIONS & USAGE

    For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes.

  • WARNINGS

    *For extemal use only.
    *Flammable. keep away from fire or flame.

  • DO NOT USE

    Do not use " with electrocautery procedures " in the eyes. lf contact occurs, flush eyes with water.

  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • STOP USE

    *Stop use if irritation and redness develop. If condition persists consult your health care practioner.

    *Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes.One piece at a time.

  • STORAGE AND HANDLING

    Store at room temperature.

  • INACTIVE INGREDIENT

    water

  • PRINCIPAL DISPLAY PANEL

    PACKING

  • INGREDIENTS AND APPEARANCE
    POVIDONE-LODINE PREP PAD 
    povidone-lodine prep pad patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84449-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84449-002-011 g in 1 PATCH; Type 0: Not a Combination Product08/20/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/20/2024
    Labeler - SHENZHEN BENLIJU BIO-TECH CO.,LTD (551073413)
    Registrant - SHENZHEN BENLIJU BIO-TECH CO.,LTD (551073413)
    Establishment
    NameAddressID/FEIBusiness Operations
    SHENZHEN BENLIJU BIO-TECH CO.,LTD551073413manufacture(84449-002)
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