Label: MYMULIKE CORN REMOVAL PADS- corn removal pads patch

  • NDC Code(s): 83781-003-01
  • Packager: Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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  • Active Ingredient

    Salicylic acid 40%

  • Purpose

    Corn and callus remover

  • Use

    for the removal of corns from foot and hand.

  • Warnings

    for external use only

  • Do not use

    on irritated skin or any area that is infected or reddened.

  • When Using

    if product gets in eyes,flush with water for 15 minutes.
    Ask a doctor before use if you have

    ■diabetes

    ■poor blood circulation

    ■under 14 years old

    ■pregnant and lactating women

  • Stop Use

    discomfort persists.

  • Ask Doctor

    discomfort persists.

  • Keep Out Of Reach Of Children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    ■Wash affected corn and dry thoroughly.

    ■Please cut the medicated patch as a suitable size to cover your corn.

    ■Place frmly the medicated round part over the center of corn. Adhesive next to skin.

    ■Repeart the treatment as need until corn is removed. (The result may vary from person.)

    ■May soak corn in warm water for 5 minutes to assist in the removal.

  • Other information

    store between 20°to 25℃ (68°to 77℉)

  • Inactive ingredients

    hard paraffin, lanolin, phenol

  • Questions

    MYMULIKE@gmail.com

  • PRINCIPAL DISPLAY PANEL

    01

  • INGREDIENTS AND APPEARANCE
    MYMULIKE CORN REMOVAL PADS 
    corn removal pads patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83781-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PHENOL (UNII: 339NCG44TV)  
    LANOLIN (UNII: 7EV65EAW6H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83781-003-0124 in 1 BOX; Type 0: Not a Combination Product11/05/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03011/05/2023
    Labeler - Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd (701762807)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd701762807label(83781-003) , manufacture(83781-003)
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