Label: GOODNITES WART REMOVER- salicylic acid liquid

  • NDC Code(s): 85578-001-01
  • Packager: Zhengzhou Hangrui Network Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 22, 2025

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  • ACTIVE INGREDIENT

    Salicylic Acid

  • PURPOSE

    Wart remover

  • INDICATIONS & USAGE

    For removing common warts and plantar warts.

  • WARNINGS

    For external use only

  • WHEN USING

    When using this product, avoid contact witheyes. lf the product gets into your eyes, rinsewith water for 15 minutes. Avoid inhalingfumes. Close the cap tightly and store atroom temperature, away from heat sources

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact aPoison Control Center(1-800-222-1222)right away.

  • DOSAGE & ADMINISTRATION


    1. Clean and soften the affected
    Area with warm water and dry it.
    2.Apply the wart remover to each affected areausing the disposable applicator.Apply once in the morning and once in the
    3.evening, daily.

  • INACTIVE INGREDIENT

    BORNEOL
    GLYCERIN
    PODOFILOX
    POLYETHYLENE GLYCOL, UNSPECIFIED
    WATER

  • PRINCIPAL DISPLAY PANEL

    label1

  • INGREDIENTS AND APPEARANCE
    GOODNITES WART REMOVER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85578-001
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    PODOFILOX (UNII: L36H50F353)  
    BORNEOL (UNII: M89NIB437X)  
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85578-001-011 in 1 BOX04/23/2025
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02804/23/2025
    Labeler - Zhengzhou Hangrui Network Technology Co., Ltd. (700094663)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhengzhou Hangrui Network Technology Co., Ltd.700094663manufacture(85578-001)
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