Label: BIOPURE MEDICATED WART REMOVER STRIPS- salicylic acid, wart remover plaster

  • NDC Code(s): 69070-308-01
  • Packager: Zhejiang Dingtai Pharmaceutical Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 2, 2024

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  • Active ingredient

    Salicylic Acid 40%

  • Purpose

    Wart Remover

  • Uses

    • for the removal of common plantar warts
    • the common wart is easily recognized by the rough "cauliflower-like" appearance of the surface
    • the plantar wart is recognized by its location only on the bottom of the foot, its tenderness and interruption of the footprint pattern
  • Warnings

    For external use only.

    Stop use and ask a doctor if

    discomfort persists.

    Do not use

    on irritated skin or on any area that is infected or reddened

    on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes

    if you have diabetes or poor blood circulation

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • wash affected area: may soak wart in warm water for 5 minutes
    • dry area thoroughly
    • peel off backing paper
    • adhere medicated patch directly over wart
    • repeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks
  • Other information

    store between 59º and 86°F (15º and 30ºC)

  • Inactive ingredients

    lanolin, paraffin, petrolatum

  • Questions?

    please call 1-718-975-2586

  • biopure. Medicated WART REMOVER STRIPS Maximum Strength 7 COUNT — Single step method cushion conceals & protects while removing warts

    Wart Remover Strips

  • INGREDIENTS AND APPEARANCE
    BIOPURE MEDICATED WART REMOVER STRIPS 
    salicylic acid, wart remover plaster
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69070-308
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.4 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    LANOLIN (UNII: 7EV65EAW6H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69070-308-011 in 1 BOX04/19/2024
    17 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03004/19/2024
    Labeler - Zhejiang Dingtai Pharmaceutical Co., Ltd (420598724)
    Registrant - QUEST USA CORP (079869689)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Dingtai Pharmaceutical Co., Ltd420598724manufacture(69070-308)
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