Label: SOUTH MOON MELITTIN JOINT SOOTHING GEL gel

  • NDC Code(s): 84732-055-01
  • Packager: Dongguan Haiyi Technology Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 20, 2024

If you are a consumer or patient please visit this version.

  • Active ingredient

    BEE VENOM

    GLUCOSAMINE

  • Inactive ingredient

    AQUA,CURCUMIN,EICOSAPENTAENOIC ACID,CHOLE-CALCIFEROL

  • Purpose section

    1.Solve various joint problems

    2.passed the USA FDAapproved

    3.Effectively relieves arthritis pain

    4.Does not contain anyharmful ingredients.

  • Warning

    Please keep out of reachof children. Do notswallow.Please clean yourhands before use to ensurethe best results from theproduct. Discontinue useif signs of irritation or rashoccur. Store in a cool and dry place.

  • stop use

    This product may cause allergic reactions in asmall number of people.
    lf youexperience any discomfort,please stop using it immediately.

  • not use

    Not suitable for use by children, pregnantor breast feeding people.

  • OUT OF CHILDREN

    KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

  • HOW TO USE

    1. Clean and dry the skin onthe joints.

    2. Take an appropriateamount of gel and apply itevenly on the joints.

    3. Gently massage withhands in circular motionuntil absorbed.

    4. Daily use can get betterresults.

  • Dosage

    take an appropriateamount,Use 2-3 times a week

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SOUTH MOON MELITTIN JOINT SOOTHING GEL 
    south moon melittin joint soothing gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84732-055
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M) APIS MELLIFERA VENOM1 mg  in 20 g
    GLUCOSAMINE (UNII: N08U5BOQ1K) (GLUCOSAMINE - UNII:N08U5BOQ1K) GLUCOSAMINE1 mg  in 20 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CURCUMIN (UNII: IT942ZTH98)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    ICOSAPENT (UNII: AAN7QOV9EA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84732-055-0120 g in 1 TUBE; Type 0: Not a Combination Product10/21/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01610/21/2024
    Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dongguan Haiyi Technology Co.,Ltd.722030807manufacture(84732-055)