Label: GZE WATERY SUN GEL- centella asiatica extract, hyaluronic acid gel

  • NDC Code(s): 83566-121-01
  • Packager: Guangzhou Yilong Cosmetics Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 31, 2024

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  • Purpose.

    sunscreen

  • Active ingredients.

    Centella Asiatica Extract 15.17%

    Sodium Hyaluronate 10%

    Tocopherol 1%

    Glycerin 1%

  • Uses.


    Gently apply to face, neck, & arms as the last step of your skincare routine.

  • Warnings

    For external use only.

  • Stop use and ask a doctor if

    rash occurs.

  • Do not use

    on damaged or broken skin.

  • When using this product

    keep out of eyes. Rinse with water to remove.

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENT

    GLYCERIN
    SODIUM ACETYLATED HYALURONATE
    HYALURONIC ACID

    WATER
    PEG-9 DIGLYCIDYL ETHERISODIUM HYALURONATE CROSSPOLYMER
    TOCOPHEROL

  • DOSAGE & ADMINISTRATION


    Squeeze out an appropriate amount of the watery sun gel,gently apply to face, neck, & arms as the last step of your skincare routine.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    GZE WATERY SUN GEL 
    centella asiatica extract, hyaluronic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83566-121
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U) (CENTELLA ASIATICA WHOLE - UNII:7M867G6T1U) CENTELLA ASIATICA WHOLE15.17 mg  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    WATER O-15 (UNII: 63M8RYN44N)  
    PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83566-121-0150 g in 1 TUBE; Type 0: Not a Combination Product12/20/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/20/2023
    Labeler - Guangzhou Yilong Cosmetics Co.,Ltd. (712647107)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yilong Cosmetics Co.,Ltd.712647107manufacture(83566-121)
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