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Salicylic Acid Corn Remover (ASO Pharmaceutical Co. Ltd.)

Available Formats

Dosage Form Package Information Links
STRIP 1 POUCH in 1 BOX (51511-514-01) > 6 STRIP in 1 POUCH Label Information
STRIP 2400 POUCH in 1 BOX (51511-514-06) > 6 STRIP in 1 POUCH Label Information

Complete Salicylic Acid Corn Remover Information

  • Active ingredient

    Salicylic acid 40%


  • Purpose

    Corn remover


  • Uses

    • for the removal of corns.
    • relieves pain by removing corns

  • Warnings

    For External Use Only

    Do not use
    • on irritated skin
    • on any area that is infected or reddened
    • if you have poor blood circulation
    • if you are diabetic

    Stop use and ask a doctor if

    discomfort lasts

    Keep out of reach of children.

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.


  • Directions

    • Wash affected area and dry thoroughly
    • Remove medicated pad from backing paper by pulling from center of pad
    • Apply
    • After 48 hours, remove medicated pad
    • Repeat 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 at room temperature
    • avoid excessive heat 99ºF (37ºC)

  • Inactive ingredients

    lanolin, polybutene, rosin ester, rubber


  • SPL UNCLASSIFIED SECTION

    Distributed by:

    ASO LLC
    Sarasota, FL 34240

    Made in Japan

    *This product is not manufactured or distributed by he Bayer Corporation, owners of the registered trademark Dr. Scholl’s®.


  • Principal Display Panel

    Compare to the active ingredient in Dr. Scholl’s®*

    ONE STEP

    CORN REMOVER

    MAXIMUM STRENGTH

    SALICYLIC ACID 40%

    • Cushions & helps relieve pain
    • Convenient 1-step bandage
    • Waterproof

    6 MEDICATED BANDAGES

    Label


  • INGREDIENTS AND APPEARANCE
    SALICYLIC ACID CORN REMOVER 
    salicylic acid strip
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51511-514
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 40 mg
    Inactive Ingredients
    Ingredient Name Strength
    LANOLIN (UNII: 7EV65EAW6H)  
    NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51511-514-01 1 in 1 BOX 02/01/2010
    1 6 in 1 POUCH; Type 0: Not a Combination Product
    2 NDC:51511-514-24 2400 in 1 CARTON 02/01/2010
    2 200 in 1 TRAY
    2 6 in 1 POUCH; Type 0: Not a Combination Product
    3 NDC:51511-514-18 1800 in 1 CARTON 01/08/2010
    3 150 in 1 TRAY
    3 8 in 1 POUCH; Type 0: Not a Combination Product
    4 NDC:51511-514-08 1 in 1 BOX 01/08/2010
    4 8 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part358B 01/08/2010
    Labeler - ASO Pharmaceutical Co. Ltd. (690629019)