Label: SCHOLLS WELLNESS COMPANY LLC DURAGEL CORN REMOVER- salicylic acid disc

  • NDC Code(s): 73469-0627-1
  • Packager: Scholls Wellness Company LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 3, 2024

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  • Drug Facts

    Drug Facts

  • ACTIVE INGREDIENT

    Salicylic Acid 40%..........Corn Remover

  • Purpose

    Corn Remover

  • Uses

    for the removal of corns

    relieves pain by removing corns

  • Warnings

    For external use only

  • DO NOT USE

    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

    Stop use and ask a doctor if discomfort lasts

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

  • Directions

    Directions

    wash affected area and dry thoroughly

    if necessary, cut medicated disc to fit corn

    apply medicated disc with sticky side adhering to skin

    cover medicated disc with enclosed cushion

    after 48 hours, remove medicated disc

    repeat procedure every 48 hours as needed for up to 14 days (untl corn is removed)

    may soak corn in warn water for 5 minutes to assist in removal

  • Other Information

    Other information

    store between 20º to 25ºC (68º to 77ºF)

    protect from excessive heat and temperatures above 40ºC (104ºF)

  • INACTIVE INGREDIENT

    Inactive ingredients antioxidant (CAS 991-84-4), iron oxides, mineral oil, petroleum hydrocarbon resin, silicon dioxide, synthetic polyisoprene rubber, talc

  • QUESTIONS

    Questions? 1-866-360-3226

  • PRINCIPAL DISPLAY PANEL

    Duragel Corn Remover

  • INGREDIENTS AND APPEARANCE
    SCHOLLS WELLNESS COMPANY LLC  DURAGEL CORN REMOVER
    salicylic acid disc
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73469-0627
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.4 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ANTIOXIDANT GS (UNII: 2BBL73FIEU)  
    BROWN IRON OXIDE (UNII: 1N032N7MFO)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    TALC (UNII: 7SEV7J4R1U)  
    WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73469-0627-16 in 1 CARTON01/01/2021
    11 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03001/01/2021
    Labeler - Scholls Wellness Company LLC (117174744)
    Registrant - Scapa Tapes North America LLC (079995435)
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