Label: MQUPIN CORN REMOVAL PADS- corn removal pads patch

  • NDC Code(s): 83781-001-01, 83781-001-02, 83781-001-03
  • 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,calluses and common warts
    relieves pain by removing corns and calluses

  • Warnings

    ■ For external use only

    ■Keep away from fire and flame

  • 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.

  • Stop Use

    discomfort persists

  • Ask Doctor

    Ask a doctor before use if you have

    ■diabetes

    ■ poor blood circulation

  • Keep Out Of Reach Of Children

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

  • Directions

    ■ Wash affected area:may soak wart in warm water for 5 minutes and and dry the area Remove bandage strips by peeling backing off

    ■lf necessary,cut medicated patch to fit wart

    ■Carefully apply medicated plaster

    ■Repeat procedure

    ■Every 48 hours as needed (until wart is removed)for up to 12 weeks

  • Other information

    ■ store between 20°to 25°C (68° to 77°F)

  • Inactive ingredients

    hard paraffin,lanolin,phenol

  • Questions

    mqupin86@gmail.com

  • PRINCIPAL DISPLAY PANEL

    0102

  • INGREDIENTS AND APPEARANCE
    MQUPIN CORN REMOVAL PADS 
    corn removal pads patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83781-001
    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:83781-001-0124 in 1 BOX; Type 0: Not a Combination Product11/05/2023
    2NDC:83781-001-0238 in 1 BOX; Type 0: Not a Combination Product11/05/2023
    3NDC:83781-001-0348 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., Ltd701762807manufacture(83781-001) , label(83781-001)
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