Label: SALICYLIC ACID- medicated corn removers 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 February 19, 2021

If you are a consumer or patient please visit this version.

  • Active ingredient

    Salicylic acid 40%

  • ​Purpose

    Corn Remover

  • ​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, or any area that is infected or reddened

    Stop Use and ​Ask a doctor 

    if discomfort persists

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wash affected area and dry area thoroughly
    • if necessary, cut medicated patch to fit corn
    • apply adhesive side down of medicated patch onto corn
    • cover medicated patch with pad
    • after 48 hours, remove medicated patch
    • repeat 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

    TopCare
    Medicated

    Corn

    Removers

    SALICYLIC ACID 40%

    • Effective Corn Removal Treatment
    • Cushions Against Pressure & Friction

    9 PADS | 9 MEDICATED PATCHES

    corn remover

  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID 
    medicated corn removers patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 9 
    Inactive Ingredients
    Ingredient NameStrength
    POLYVINYL ALCOHOL (UNII: 532B59J990)  
    VINYL ACETATE (UNII: L9MK238N77)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:36800-021-099 in 1 PACKAGE; Type 0: Not a Combination Product01/03/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358F01/03/2012
    Labeler - Topco Associates LLC (006935977)