Label: PURESKIN WART REMOVER GEL gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 15, 2024

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  • Active Ingredient

    Salicylic Acid 17%

  • Purpose

    Wart Remover

  • Use

    Plantar Warts, Flat Warts, Common Warts

  • Warnings

    For external use only.

  • Do not use

    if you are diabetic, have poor blood circulation, or are allergic to this product
    if you are pregnant or breast-feeding
    on face, eye, genitals, mucous membranes, or healthy skin.
    on moles, birthmarks, and warts with hair growing from them
    on irritated, infected, or reddened skin

  • When Using

    Flush with water immediately if it gets into your eyes

  • Stop Use

    and ask a doctor if discomfort persists.

  • Ask Doctor

    If you are pregnant, breast-feeding, or have any underlying conditions.

  • Keep Oot Of Reach Of Children

    If swallowed, get medical help or contact a poison Control Center immediately.

  • Directions

    1. Wash affected area, may soak the wart with warm water for 5 minutes.
    2. Dry it thoroughly.
    3. Apply a small drop to cover each wart.
    4. Let dry and repeat this procedure once or twice daily until the wart is removed.

  • Other information

    Close the cap tightly and keep away from heat above 104°F.

  • Inactive ingredients

    Water, Sophora Flavescens, Prunus Mume (sieb.), Cnidium Monnieri (L.) Cuss, Crocus Sativus L., Gleditsia Sinensis Lam., Cortex Dictamni, Borneol, Kochia Scoparia Whole

  • Questions

    www.pureskinsupport.com, info@pureskinsupport.com

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    PURESKIN WART REMOVER GEL 
    pureskin wart remover gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83565-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID17 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DICTAMNUS DASYCARPUS ROOT BARK (UNII: LA97176ILS)  
    PRUNUS MUME WHOLE (UNII: 3RSQ38B1JI)  
    GLEDITSIA SINENSIS WHOLE (UNII: FS3UB95UTG)  
    WATER (UNII: 059QF0KO0R)  
    CNIDIUM MONNIERI WHOLE (UNII: GYR30735RE)  
    BORNEOL (UNII: M89NIB437X)  
    BASSIA SCOPARIA WHOLE (UNII: 240G38P85Z)  
    SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)  
    CROCUS SATIVUS WHOLE (UNII: Z5C927G4XF)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83565-010-0115 mL in 1 TUBE; Type 0: Not a Combination Product07/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02807/15/2024
    Labeler - Stellans Inc. (111157321)
    Establishment
    NameAddressID/FEIBusiness Operations
    Stellans Inc.111157321manufacture(83565-010) , label(83565-010)
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