Label: WART REMOVER PATCHES- salicylic acid 12% patch

  • NDC Code(s): 85839-009-01
  • Packager: Shenzhen Finona Information Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 1, 2025

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  • ACTIVE INGREDIENT

    Salicylic acid 12%

  • PURPOSE

    Wart Remover

  • INDICATIONS & USAGE

    For the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-ike' appearance of the sruface

  • 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 form them
    On mucous membranes

  • WHEN USING

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

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    wash affected area may soak wart in warm water for 5 minutes dryarea thoroughlyremove bandage strips by peeling backing offif necessary, cut medicated patch to fit wartcarefully apply medicated plasterrepeat procedure every 48 hours as needed(until wart is removed)for up to 12 week

  • INACTIVE INGREDIENT

    hard paraffin
    lanolin
    phenol
    borneol
    crocus sativus L
    gleditsia sinensis Lam

  • PRINCIPAL DISPLAY PANEL

    label1

  • INGREDIENTS AND APPEARANCE
    WART REMOVER PATCHES 
    salicylic acid 12% patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85839-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.12 g
    Inactive Ingredients
    Ingredient NameStrength
    GLEDITSIA SINENSIS WHOLE (UNII: FS3UB95UTG)  
    BORNEOL (UNII: M89NIB437X)  
    PHENOL (UNII: 339NCG44TV)  
    LANOLIN (UNII: 7EV65EAW6H)  
    CROCUS SATIVUS WHOLE (UNII: Z5C927G4XF)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85839-009-01144 in 1 BOX09/01/2025
    11 in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02809/01/2025
    Labeler - Shenzhen Finona Information Technology Co., Ltd (511271543)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Finona Information Technology Co., Ltd511271543manufacture(85839-009)
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