Label: WART REMOVER PATCHS- wart remover patch

  • NDC Code(s): 84168-003-01
  • Packager: Gaozhou Chapin Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 22, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Salicylic acid 20%

  • PURPOSE

    Wart Remover

  • USE

    For the removal of common warts. The common wart is easily recognized by the rough ‘cauliflower-like’ appearance of the surface.

  • WARNINGS

    For external use only.

  • DO NOT USE

    on irritated, infected or reddened skin
    on genital warts and warts on the face
    on moles, birthmarks and warts with hair growing from them
    on mucous membranes

  • KEEP OUT OF REACH OF CHILDREN

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

  • DIRECTIONS

    wash affected area: may soak wart in warm water for 5 minutes
    dry area thoroughly
    remove bandage strips by peeling backing off
    If necessary, cut medicated patch to fit wart
    carefully apply medicated plaster
    repeat procedure every 48 hours as needed (until wart is removed) for up to 12 week

  • WHEN USING

    Ask a doctor before use if you have
    diabetes poor blood circulatio

  • OTHER INFORMATION

    Store between 59° and 86°F (15° and 30°C).

  • INACTIVE INGREDIENTS

    Ethylhexyl Acrylate ·Polyethylene Terephthalate

  • DOSAGE & ADMINISTRATION SECTION

    One patch per day, each patch contains1 mg of tolnaftate

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    WART REMOVER PATCHS 
    wart remover patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84168-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID200 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG) 380 mg  in 1 g
    POLYETHYLENE TEREPHTHALATE (INTRINSIC VISCOSITY 0.40-0.70) (UNII: Y78AJD3DED) 420 mg  in 1 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84168-003-0125 g in 1 BOX; Type 0: Not a Combination Product03/22/202403/21/2029
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02803/22/202403/21/2029
    Labeler - Gaozhou Chapin Technology Co., Ltd (715573719)
    Establishment
    NameAddressID/FEIBusiness Operations
    Gaozhou Chapin Technology Co., Ltd715573719manufacture(84168-003)