Label: WALGREENS CORN REMOVER- salicylic acid strip

  • NDC Code(s): 0363-3063-01, 0363-3063-03
  • Packager: WALGREENS Co
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 20, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Salicylic acid 40%

  • Purpose

    Corn remover

  • Uses

    • For the removal of corns
    • relieves pain by removing corns
  • Warnings

    For external use only
    Use only as directed

    Do Not Use

    • if you are diabetic
    • on irritated, broken or infected skin
    • if you have poor blood circulation

    If discomfort persists, see your doctor or podiatrist.

    KEEP OUT OF REACH OF CHILDREN.

    If swallowed, get medical help or contact a Poison Control center immediately.

  • Directions

    • Wash affected area. Soak in warm water for 5 minutes if desired. Dry thoroughly.
    • Remove bandage from backing
    • Apply with medicated area directly over corn
    • After 48 hours, remove medicated bandage
    • Repeat procedure every 48 hours as needed (until corn is removed) for up to 14 days
  • Other Information

    Store between 59° and 86°F (15° and 30°C)

  • Inactive Ingredients

    Polyvinyl Alcohol, Acrylic Copolymer

  • Questions or Comments?

    CALL: 1-800-925-4733

  • SPL UNCLASSIFIED SECTION

    DISTRIBUTED BY: WALGREEN CO.
    200 WILMOT RD., DEERFIELD, IL 60015

  • PRINCIPAL DISPLAY PANEL - 6 Strip Box

    Well at

    Walgreens

    WALGREENS PHARMACIST RECOMMENDED ‡

    NEW

    MAXIMUM STRENGTH • ONE-STEP

    Corn Remover

    Strips

    Salicylic Acid 40%

    • Removes corns in as

      few as two treatments*
    • Water resistant
    • Medicated pad
    • Stays in place



    MEDICATED

    STRIPS

    Compare to Dr. Scholl's ® OneStep

    Corn Removers active ingredient ‡‡

    3063IMG

  • INGREDIENTS AND APPEARANCE
    WALGREENS CORN REMOVER 
    salicylic acid strip
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-3063
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID4.42 mg
    Inactive Ingredients
    Ingredient NameStrength
    POLYVINYL ALCOHOL (UNII: 532B59J990)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    VINYL ACETATE (UNII: L9MK238N77)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-3063-032 in 1 BOX01/01/2021
    1NDC:0363-3063-013 in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03006/01/2013
    Labeler - WALGREENS Co (008965063)
    Registrant - PEDIFIX, INC. (122271935)
    Establishment
    NameAddressID/FEIBusiness Operations
    PEDIFIX122271935pack(0363-3063) , label(0363-3063)
    Establishment
    NameAddressID/FEIBusiness Operations
    AKRON186569323manufacture(0363-3063)
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