Label: SALICYLIC ACID- clear medicated corn removers patch

  • NDC Code(s): 56104-258-01
  • Packager: Premier Brands of America Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 1, 2024

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  • Active ingredient

    Salicylic acid 40% w/w

  • Purpose

    Corn remover

  • Use

    • for the removal of corns
  • Warnings

    For external use only.

    Do not use

    • if you are a diabetic
    • if you 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 disc to fit the corn.
    • carefully apply the medicated with sticky side onto the corn
    • cover the medicated disc with the center of the bandage strip.
    • after 48 hours, remove the medicated bandage strip.
    • 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 59° and 86°F (15° and 30°C)

  • Inactive ingredients

    acrylic adhesive, polyethylene foam.

  • Questions?

    Call 1-866-964-0939

  • Principle Display Panel

    Premier Solutions

    Medicated Clear

    Corn Removers

    SALICYLIC ACID 40%

    MAXIMUM

    STRENGTH

    Effective corn removal treatment

    Conceals & protects

    Medicated disc, no-mess application

    6 MEDICATED DISCS | 6 CLEAR STRIPS

    Image 1

  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID 
    clear medicated corn removers patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56104-258
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 12 
    Inactive Ingredients
    Ingredient NameStrength
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    VINYL ACETATE (UNII: L9MK238N77)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56104-258-016 in 1 PACKAGE; Type 0: Not a Combination Product02/22/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03002/22/2022
    Labeler - Premier Brands of America Inc. (117557458)
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