Label: W.SKIN HYALURONIC TONER- sodium hyaluronate liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 8, 2021

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  • ACTIVE INGREDIENT

    Ethylhexyl Methoxycinnamate

  • INACTIVE INGREDIENT

    Isoamyl p-Methoxycinnamate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Zinc Oxide, Propylene Glycol, Glycerin, Sodium Hyaluronate, Glyceryl Stearate, Glyceryl Stearate SE, Sorbitan Stearate, Sorbitan Sesquioleate, 1,2-Hexanediol, Polysorbate 60, Isopropyl Myristate, Caprylic/Capric Triglyceride, Cyclomethicone, Phenyl Trimethicone, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Adenosine, Beeswax

  • PURPOSE

    It has a strong sun block and waterproof function. It contains a large amount of hyaluronic acid to prevent evaporation of moisture from the skin.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    At the end of skin care, take an appropriate amount and apply evenly over the skin

  • WARNINGS

    If there are any abnormal symptoms or side effects such as red spots, swelling, or itching due to direct sunlight during or after using cosmetics. 2. Avoid using areas with wounds. 3. Precautions for storage and handling. 3.1) Keep out reach of children. 3.2) Keep it out of direct sunlight.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    W.SKIN HYALURONIC TONER 
    sodium hyaluronate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74997-0019
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74997-0019-1250 mL in 1 BOTTLE; Type 0: Not a Combination Product05/08/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/08/2021
    Labeler - J&J COMPANY (688995236)
    Registrant - J&J COMPANY (688995236)
    Establishment
    NameAddressID/FEIBusiness Operations
    J&J COMPANY688995236manufacture(74997-0019) , label(74997-0019) , pack(74997-0019)
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