Label: WART REMOVER- salicylic acid liquid

  • NDC Code(s): 84302-001-01
  • Packager: Shenzhen Hanchuan e-commerce Co., Ltd
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated May 9, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    WART REMOVER

  • ACTIVE INGREDIENT

    Salicylic acid 1%

  • PURPOSE

    Wart Remover

  • INDICATIONS & USAGE

    For the removal of genital,plantar, common, and flat warts.
    The common wart is easilyrecognized by the rough "cauli-flower-like" appearance of thesurface.
    The plantar wart is recognizedby its location only on thebottom of the foot, its tender-ness and the interruption of thefootprint pattern.

  • WARNINGS

    For extemal use only.

    Keep away from fire and flame.

  • WHEN USING

    Avoid contact with eyes. If theproduct gets into the eye, flushwith water for 15 minutese.
    Avoid inhaling vapors.
    Cap the tube tightly.
    Out of direct sunlight and storeat room temperature away fromheat.

  • STOP USE

    lf discomfort persistself you have diabetes or poor blood circulation.

  • KEEP OUT OF REACH OF CHILDREN

    If swallowedget medical help orcontact a Poison Control Center(1-800-222-1222)right away

  • DOSAGE & ADMINISTRATION

    .Wash the affectod area May soakthe wart in warm water for 5minutes Dry area thoroughly Usingthe applicator (cottonswab), apply alayer of ointment to sufficientlycover each wart ·Allow it to fullyabsorb and cover it with a bandageas needed Repeat this procedureonce or twice daily as needed (untilthe wart is removed) for up to 12weeks

  • STORAGE AND HANDLING

    Out of direct sunlight and storeat room temperature away fromheat.

  • INACTIVE INGREDIENT

    Water
    Alcohol
    Glycerin
    Propylene Glycol
    Dimethyl Isosorbide
    Erythritol
    Phenoxyethanol
    Aloe Yohjyu Matsu Ekisu
    Glyceryl Glucoside
    Portulaca Oleracea Extract
    Gentiana Scabra Root Extract
    Xanthan Gum
    Retinoic Acid
    Dipotassium Glycyrrhizate

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    WART REMOVER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84302-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GENTIANA SCABRA ROOT (UNII: GXZ33VNT92)  
    PURSLANE (UNII: M6S840WXG5)  
    GLYCERYL GLUCOSIDE (UNII: 3297VXM8Z6)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE (UNII: V5VD430YW9)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    WATER (UNII: 059QF0KO0R)  
    ERYTHRITOL (UNII: RA96B954X6)  
    TRETINOIN (UNII: 5688UTC01R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84302-001-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product05/09/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02805/09/2024
    Labeler - Shenzhen Hanchuan e-commerce Co., Ltd (449984812)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Hanchuan e-commerce Co., Ltd449984812manufacture(84302-001)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!