Label: SOUTH MOON CORN REMOVAL PLASTER- glycerin plaster

  • NDC Code(s): 84660-062-01
  • Packager: Guangdong Ximonth Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 2, 2024

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  • Active Ingredient(s)

    SOPHORA FLAVESCENS ROOT、SAFFLOWER、GLYCYRRHIZA GLABRA、ALOE VERA LEAF

  • Purpose

  • Use

    1.Cleanse and dry the affected area.
    2.Apply the cream to the surrounding skin Cream.
    3.Apply it 2 times Daily.

  • Warnings

    Please keep out of reach of children.Do not swallow.Please clean your hands before use to ensure the best results from the product.Discontinue use if signs of irritation or rash occur.Store in a cool and dry place.

  • Do not use

    Discontinue use if signs of irritation or rash occur.

  • Stop Use

    Discontinue use if signs of irritation or rash occur.

  • KEEP OUT OF REACH OF CHILDREN

    Please keep out of reach of children. Do not swallow.

  • STORAGE AND HANDLING

    Store in a cool and dry place.

  • INACTIVE INGREDIENT

    GLYCERIN

  • DOSAGE & ADMINISTRATION

  • INDICATIONS & USAGE

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SOUTH MOON CORN REMOVAL PLASTER 
    glycerin plaster
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84660-062
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (GLYCYRRHIZA GLABRA - UNII:2788Z9758H) GLYCYRRHIZA GLABRA2 g  in 16 g
    SAFFLOWER (UNII: 4VBL71TY4Y) (SAFFLOWER - UNII:4VBL71TY4Y) SAFFLOWER4 g  in 16 g
    ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X) ALOE VERA LEAF2 g  in 16 g
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) (SOPHORA FLAVESCENS ROOT - UNII:IYR6K8KQ5K) SOPHORA FLAVESCENS ROOT4 g  in 16 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 4 g  in 16 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84660-062-0116 g in 1 BOX; Type 1: Convenience Kit of Co-Package11/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01611/02/2024
    Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)
    Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Ximonth Technology Co., Ltd.699436264manufacture(84660-062)