Label: CLEAR GEL CORN REMOVER- salicylic acid patch

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 29, 2024

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  • Active Ingredient

    Salicylic acid 40%

  • Purpose

    Corn Remvoer

  • Uses

    • for the removal of corns
    • relieves pain by removing corns
  • 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

    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 and dry thoroughly
    • apply adhesive side down of medicated disc on to the corn
    • cover the medicated disc with corn cushion
    • after 48 hours, remove medicated disc
    • repeat this procedure every 48 hours as needed for up to 14 days (until corn is removed)
    • may soak corn in warm water for 5 minutes to assist in removal
  • Other Information

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

  • Inactive Ingredients

    acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

  • Questions

    Call 1-866-964-0939

  • Principal Display Panel

    CORE VALUES

    Medicated

    Clear Gel Corn Removers

    SALICYLIC ACID 40%

    Maximum strength

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

    6 CUSHIONS

    6 MEDICATED DISCS

    Clear Gel Corn Removers

  • INGREDIENTS AND APPEARANCE
    CLEAR GEL CORN REMOVER 
    salicylic acid patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63940-165
    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
    VINYL ACETATE (UNII: L9MK238N77)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63940-165-066 in 1 PACKAGE; Type 0: Not a Combination Product01/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03001/01/2018
    Labeler - Harmon Store Inc. (804085293)
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