Label: SANDAWHA VITAMIN C BRIGHTENING ESSENCE- ascorbyl glucoside liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72289-0013-1 - Packager: SKINCURE INC
- 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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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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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
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SANDAWHA VITAMIN C BRIGHTENING ESSENCE
ascorbyl glucoside liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72289-0013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) (ASCORBYL GLUCOSIDE - UNII:2V52R0NHXW) ASCORBYL GLUCOSIDE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength PANTHENOL (UNII: WV9CM0O67Z) NIACINAMIDE (UNII: 25X51I8RD4) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72289-0013-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/23/2020 Labeler - SKINCURE INC (557830240) Registrant - SKINCURE INC (557830240) Establishment Name Address ID/FEI Business Operations SKINCURE INC 557830240 label(72289-0013) , manufacture(72289-0013)