Label: CLEAR GEL CORN REMOVER- salicylic acid patch

  • NDC Code(s): 68016-444-12
  • Packager: Chain Drug Consortium, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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  • Active Ingredient

    Salicylic acid 40%

  • Purpose

    Wart Remvoer

  • Uses

    • for the removal of common warts. the common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface.
  • Warnings

    For external use only.

    Do not use

    • if you are diabetic
    • have poor blood circulation
    • on irritated skin, on any area that is infected or reddened
    • on genital warts and warts on the face
    • on moles, birthmarks and warts with hair growing from them
    • on mucous membranes

    Stop use and ask doctor

    if discomfort persist

    Keep out of reach of children.

    If, swallowed , get medical help or cotnact a poison Control Center right away.

  • Directions

    • wash affected area, may soak wart in warm water for 5 minutes
    • dry area thoroughly
    • if necessary, cut medicated disc to fit wart
    • carefully apply adhesive side down of disc onto the wart
    • cover disc with cushion to conceal area
    • repeart this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks
  • Other Information

    store between 59°F to 86°F (15°F to 30°F)

  • Inactive Ingredients

    acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

  • Questions

    Call 1-866-964-0939

  • Principal Display Panel

    Premier Value

    Medicated

    Clear Gel Wart Removers

    SALICYLIC ACID 40%

    Maximum strength

    • Effective wart removal treatment
    • Clear gel cushions affected area
    • Thin, flexible bandage conceals and protects

    9 CUSHIONS

    12 MEDICATED DISCS

    image 1

  • INGREDIENTS AND APPEARANCE
    CLEAR GEL CORN REMOVER 
    salicylic acid patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-444
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 6 
    Inactive Ingredients
    Ingredient NameStrength
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    VINYL ACETATE (UNII: L9MK238N77)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68016-444-126 in 1 PACKAGE; Type 0: Not a Combination Product01/19/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03001/01/2018
    Labeler - Chain Drug Consortium, LLC (101668460)
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