Label: WART REMOVER liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 13, 2023

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  • Active Ingredient

    salicylic acid 12%

  • Purpose

    Wart remover

  • Use

    for the removal ot common and plantar warts
    the common wart ls 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 the
    interruption of the footprint pattern

  • Warnings

    For external use only
    Keep away from fire and flame

  • When Using

    avoid contact with eyes. If the product gets into the
    eye lush with water for 15 minutes
    avoid inhaling vapers
    cap the bottle tightly

  • Stop Use

    If discomfort persists

  • Ask Doctor

    If you have diabetes or poor blood circulation

  • Keep Oot Of Reach Of Children

    Keep Oot Of Reach Of Children

  • Directions

    wash the affected area
    mey soak the wart in warm water tor 5 minutes
    Gry area thoroughly
    using the applicator(cotton swab), apply a layer at
    Gintment to sufficiently cover each wart
    allow it to fully absorb and cover it with a bandage as
    needed.
    repeat this procedure once or twice daily as needed
    (until the wart is removed) for up to 12 weeks

  • Inactive ingredients

    Watery, Sodiurn bicarbonate
    Propylene glycol, Ethanol, Frutus cnidil,
    Kuhrseng, Pursiane, The rhizome of
    large-headed atractylodes, Radix angelicae,
    Pericarpiur citri reticulatae, Asarum,
    Fructus forsythiae, Bamboo leat, Platycodon
    grandiflorur, xanthan gum

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    WART REMOVER 
    wart remover liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83299-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE12 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SURINAMINE (UNII: AIQ58N56TM)  
    PURSLANE (UNII: M6S840WXG5)  
    ATRACTYLODES LANCEA WHOLE (UNII: HT7Q1X5HVM)  
    CITRUS MAXIMA FRUIT RIND (UNII: 5NX3G75CA6)  
    FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5)  
    BAMBUSA VULGARIS LEAF (UNII: EMY54R518C)  
    PLATYCODON GRANDIFLORUS WHOLE (UNII: WC73QE9274)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CNIDIUM MONNIERI WHOLE (UNII: GYR30735RE)  
    PLATYCODON GRANDIFLORUM LEAF (UNII: 2L64H2X8DY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83299-007-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02806/13/2023
    Labeler - Consilii LLC (118891890)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consilii LLC118891890manufacture(83299-007) , label(83299-007)
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