Label: THE SKIN HOUSE HYALURONIC 6000 AMPOULE- sodium hyaluronate liquid

  • NDC Code(s): 73590-0020-1
  • Packager: NOKSIBCHO cosmetic Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated March 16, 2020

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  • ACTIVE INGREDIENT

    Sodium Hyaluronate

  • INACTIVE INGREDIENT

    Water
    Sodium Hyaluronate
    Phenoxy ethanol
    Glycerin
    Butylene glycol
    Betaine
    Alcohol
    1,2-Hexanediol
    PPG-26-Buteth-26
    PEG-40 Hydrogenated Castor Oil
    Arginine
    Squalane
    Camellia Sinensis Leaf Extract
    Hydrolyzed Collagen
    Dipotassium Glycyrrhizate
    Sodium Citrate
    Glyceryl Acrylate/Acrylic Acid Copolymer
    Propylene Glycol
    PVM/MA Copolymer
    Carbomer
    Xanthan GUM
    Solanum Lycopersicum (Tomato) Fruit Extract
    Paeonia Lactiflora Bark/Sap Extract
    Lonicera Japonica (Honeysuckle) Flower Extract
    Myrciaria Dubia Fruit Extract
    Euterpe Oleracea Fruit Extract
    Ardisia Crispa Extract
    Rubus Coreanus Fruit Extract
    Phellinus Linteus Extract
    Aloe Barbadensis Leaf Extract
    Nelumbo Nucifera Leaf Extract
    Citric Acid
    Adenosine
    Disodium EDTA
    Panax ginseng culture extract
    Caprylyl Glycol
    Phaseolus Radiatus Seed Extract
    Ethylhexylglycerin
    Gardenia Florida Fruit Extract
    Parfum

  • PURPOSE

    anti-wrinkle function

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    apply proper amount and gently massage

  • WARNINGS

    For external use only
    When using this product

    ■ if the following symptoms occurs after use, stop use and consult with a skin specialist

    red specks, swelling, itching

    ■ don’t use on the part where there is injury, eczema, or dermatitis

    Keep out of reach of children

    ■ if swallowed, get medical help or contact a person control center immediately

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    THE SKIN HOUSE HYALURONIC 6000 AMPOULE 
    sodium hyaluronate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73590-0020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73590-0020-130 mL in 1 BOTTLE; Type 0: Not a Combination Product03/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/14/2020
    Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175)
    Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175)
    Establishment
    NameAddressID/FEIBusiness Operations
    NOKSIBCHO cosmetic Co., Ltd.690182175manufacture(73590-0020)
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