Label: EQUATE CORN AND CALLUS REMOVER- salicylic acid liquid

  • 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 October 4, 2010

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Salicylic acid 17.6% w/w

  • Purpose

    Corn/Callus remover

  • Use

    for the removal of corn and calluses

  • Warnings

    For external use only.

    • avoid inhaling vapors
    • extremely flammable
    • keep away from fire or flame
    • cap bottle tightly and store at room temperature away from heat
    • avoid contact with eyes
    • if product gets into the eye, flush with water for 15 minutes

    Do not use

    this product

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

    When using this product

    • 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 right away.

  • Directions

    • wash affected area
    • you may soak callus or corn in warm water for 5 minutes
    • dry area thoroughly
    • apply one drop at a time to cover each corn or callus
    • let dry
    • repeat procedure once or twice daily as needed for up to 14 days (until corn or callus is removed)
  • Inactive ingredients

    alcohol, flexible collodion

  • Questions?

    call 1-888-287-1915

  • PRINCIPAL DISPLAY PANEL

    Liquid Corn &
    Callus Remover
    Salicylic Acid
    0.31 FL OZ (9 mL)

    PRINCIPAL DISPLAY PANEL Liquid Corn & Callus Remover

  • INGREDIENTS AND APPEARANCE
    EQUATE CORN AND CALLUS REMOVER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-151
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID170 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    ETHER (UNII: 0F5N573A2Y)  
    ETHYLCELLULOSE (UNII: 7Z8S9VYZ4B)  
    MENTHOL (UNII: L7T10EIP3A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-151-011 in 1 BOX
    19 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart358B10/01/2010
    Labeler - Wal-Mart Stores Inc. (051957769)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aso Americas S.690629019MANUFACTURE
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