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
  • 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 23, 2023

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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 finalpart358F02/22/2022
    Labeler - Premier Brands of America Inc. (117557458)
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