Label: SOUTH MOON BEE VENOM NAIL FUNGUS REPAIRING LIQUID- glycerin liquid

  • NDC Code(s): 84983-004-01
  • Packager: Shantou South Moon Biotechnology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 27, 2025

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

  • ACTIVE INGREDIENTS

    APIS MELLIFERA VENOM、HONEY

  • PURPOSE

    Eliminates various types of fungal infections;strong antimicrobial properties to eliminate fungi;stimulate tissue regeneration;promote long-term prevention of infections

  • USES

    Use a brush to take an appropriate amount of this product and apply it evenly on the nail surface and surrounding skin. Just wait a few minutes for it to dry naturally.

  • 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 INGREDIENTS

    AQUA、
    UREA、
    SILVER CHLORIDE、
    GLYCERIN

  • INDICATIONS & USAGE

  • DOSAGE & ADMINISTRATION

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    SOUTH MOON BEE VENOM NAIL FUNGUS REPAIRING LIQUID 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84983-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M) APIS MELLIFERA VENOM0.002 g  in 10 g
    HONEY (UNII: Y9H1V576FH) (HONEY - UNII:Y9H1V576FH) HONEY0.002 g  in 10 g
    Inactive Ingredients
    Ingredient NameStrength
    SILVER CHLORIDE (UNII: MWB0804EO7) 0.05 g  in 10 g
    AQUA (UNII: 059QF0KO0R) 9.444 g  in 10 g
    UREA (UNII: 8W8T17847W) 0.5 g  in 10 g
    GLYCERIN (UNII: PDC6A3C0OX) 0.002 g  in 10 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84983-004-0110 g in 1 BOTTLE; Type 0: Not a Combination Product02/13/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01602/13/2025
    Labeler - Shantou South Moon Biotechnology Co., Ltd. (457126192)
    Registrant - Shantou South Moon Biotechnology Co., Ltd. (457126192)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shantou South Moon Biotechnology Co., Ltd.457126192manufacture(84983-004)