Label: SALICYLIC ACID- liquid corn and callus remover liquid

  • NDC Code(s): 0363-9889-10, 0363-9889-15
  • Packager: Walgreen Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • ​Active ingredient

    Salicylic acid 17%w/w

  • Purpose

    Corn and callus remover

  • Uses

    • for the removal of corns and calluses
    • relieves pain by removing corns and calluses
  • ​ ​Warnings

    For external use only.

    Flammable

    • keep away from fire or flame
    • cap bottle tightly and store at room temperature away heat

    Do not use

    • on irritated skin
    • on any area that is infected or reddened
    • if you are a diabetic
    • if you have poor blood circulation

    When using this product

    • if discomfort persists, see your doctor or podiatrist
    • avoid contact with eyes
    • avoid inhaling vapors
    • if product gets into the eyes, flush with water for 15 minutes

    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 thoroughly
    • apply one drop at a time with applicator, to sufficiently cover each corn/callus; let dry
    • use cushions with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately)
    • repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
  • Other information

    store between 20°C to 30°C (68°F to 86°F)

  • Inactive ingredients

    camphor, castro oil, ethanol, ethyl ether, nitrocellulose

  • Questions?

    Call 1-866-964-0939

  • ​Principal Display Panel

    Well at Walgreens

    Liquid Corn & Callus Remover

    Salicylic Acid 17%

    • Removes corn & calluses safely
    • Cushions against shoe friction

    3 Cushions

    0.5 FL OZ (15mL)

    WAL LiqCornCallusRem V2.jpg

    label

  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID 
    liquid corn and callus remover liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9889
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.17 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PYROXYLIN (UNII: KYR8BR2X6O)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9889-1515 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product07/09/2008
    2NDC:0363-9889-1010 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product07/09/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03007/09/2008
    Labeler - Walgreen Company (008965063)
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