Label: CLEAR GEL CORN REMOVER- salicylic acid patch

  • 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 January 18, 2023

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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
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    VINYL ACETATE (UNII: L9MK238N77)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    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 finalpart358F01/01/2018
    Labeler - Harmon Store Inc. (804085293)
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