Label: SOUTH MOON PROPOLIS PROFESSIONAL TREATMENT GEL- allantoin gel

  • NDC Code(s): 84660-034-01
  • Packager: Guangdong Ximonth Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 26, 2024

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  • Active Ingredient(s)

    GLUCOSE、CURCUMIN、EICOSAPENTAENOIC ACID、CHOLECALCIFEROL

  • Purpose

    1.His product contains a variety of active ingredients to promote blood circulation, relieve arthritis pain,and eliminate joint inflammation.
    2.Liminate cysts and edema,promote joint tissue repair,improve joint elasticity and mobility.
    3.The texture is refreshing and non-greasy, easy to be absorbed by the skin. Deep penetration to solve various joint problems.
    4.Convenient to use, long-lasting effect, safe and does not hurt the skin.

  • Use

    1.Clean the skin and dry it.
    2.Take an appropriate amount of this product and apply it evenly on the joint skin discomfort.
    3.Gently massage until fully absorbed(It is recommended to use 2-3 times a day to achieve better results)

  • 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

    Avoid freezing and excessive heat above 40C (104F) ）
    Store in a cool and dry place.

  • INACTIVE INGREDIENT

    ALLANTOIN

  • DOSAGE & ADMINISTRATION

  • INDICATIONS & USAGE

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SOUTH MOON PROPOLIS PROFESSIONAL TREATMENT GEL 
    allantoin gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84660-034
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) ANHYDROUS DEXTROSE5 g  in 20 g
    CURCUMIN (UNII: IT942ZTH98) (CURCUMIN - UNII:IT942ZTH98) CURCUMIN4 g  in 20 g
    ICOSAPENT (UNII: AAN7QOV9EA) (ICOSAPENT - UNII:AAN7QOV9EA) ICOSAPENT3 g  in 20 g
    CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL2 g  in 20 g
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z) 6 g  in 20 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84660-034-0120 g in 1 BOX; Type 0: Not a Combination Product09/27/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/27/2024
    Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)
    Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Ximonth Technology Co., Ltd.699436264manufacture(84660-034)
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