Label: RESVERATROL NMN COLLAGEN SERUM liquid

  • NDC Code(s): 84732-042-01
  • Packager: Dongguan Haiyi Technology Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 13, 2024

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  • Active ingredient

    Resveratrol

  • Inactive ingredient

    Aqua,,Pantoea Vagans/Nicotinamide Mononucleotide Ferment Extract Filtrate Extract, sodium Hyaluronate, Niacinamide.Collagen.

  • Purpose section

    stimulates the body's own collagen production and promotes the production of skin proteins such as elastin and fibrillin. Makes skin appear plumper and firmer.Rejuvenates skin, improves elasticity.provides an even, radiant complexion, is hydrating, non-sticky and absorbs quickly.

  • Warning

    1. Avoid direct contact with eyes. lfany discomfort occurs, stop use andrinse with plenty of water. lf thesituation is serious, seek medicaltreatment promptly.

    2. Not suitable for use by children,pregnant women or nursing mothers

    3. Store in a cool and dry place.

  • stop use

    This product may cause allergic reactions in asmall number of people.
    lf you experience 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

    After cleansing and toning, take an appropriate amount of essence and apply it evenly on your facial skin,and massage gently in circularmotions with your hands to allow it tobe absorbed.

  • Dosage

    take an appropriateamount,Use 2-3 times a week

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    RESVERATROL NMN COLLAGEN SERUM 
    resveratrol nmn collagen serum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84732-042
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RESVERATROL (UNII: Q369O8926L) (RESVERATROL - UNII:Q369O8926L) RESVERATROL1 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    NIACINAMIDE (UNII: 25X51I8RD4)  
    METHYL CARBOXYMETHYLPHENYL AMINOCARBOXYPROPYLPHOSPHONATE (UNII: K48QWH6YGJ)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84732-042-0130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product10/14/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01610/14/2024
    Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dongguan Haiyi Technology Co.,Ltd.722030807manufacture(84732-042)
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