Label: SANDAWHA VITAMIN C BRIGHTENING ESSENCE- ascorbyl glucoside liquid

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

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated November 24, 2020

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  • ACTIVE INGREDIENT

    Ascorbyl Glucoside

  • INACTIVE INGREDIENT

    Water (Aqua)
    Pentylene Glycol
    Glycerin
    Arginine
    Propanediol
    Betaine
    Niacinamide
    Panthenol
    Cellulose Gum
    Hyaluronic Acid
    Polyglyceryl-10 Myristate
    Polyglyceryl-10 Laurate
    Sorbitan Caprylate
    Hordeum Vulgare Seed Extract
    Carthamus Tinctorius (Safflower) Seed Oil
    Levulinic Acid
    Bisabolol
    Glycyrrhiza Glabra (Licorice) Root Extract
    Naringin
    Rutin
    Hesperidin
    Centella Asiatica Extract
    Polygonum Cuspidatum Root Extract
    Tocopherol
    Camellia Sinensis Leaf Extract
    Scutellaria Baicalensis Root Extract
    Rosmarinus Officinalis (Rosemary) Leaf Extract
    Chamomilla Recutita (Matricaria) Leaf Extract
    Jasminum Sambac (Jasmine) Flower Extract
    Rose Flower Oil

  • PURPOSE

    remove the appearance of dark spots and prevent unwanted skin pigmentation

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Apply liberal amount on your face. For the best results use twice daily in the morning and the evening.

  • WARNINGS

    for external use only

    do not use if sensitive to any of the ingredients

    discontinue use if signs of irritation or rash appear

    if irritation or rash persists, contact a doctor

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SANDAWHA VITAMIN C BRIGHTENING ESSENCE 
    ascorbyl glucoside liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72289-0013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) (ASCORBYL GLUCOSIDE - UNII:2V52R0NHXW) ASCORBYL GLUCOSIDE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PANTHENOL (UNII: WV9CM0O67Z)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72289-0013-130 mL in 1 BOTTLE; Type 0: Not a Combination Product11/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/23/2020
    Labeler - SKINCURE INC (557830240)
    Registrant - SKINCURE INC (557830240)
    Establishment
    NameAddressID/FEIBusiness Operations
    SKINCURE INC557830240label(72289-0013) , manufacture(72289-0013)