Label: UNIWELL NATURAL TONER- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71502-004-01, 71502-004-02 - Packager: uniwell LTD
- 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 June 14, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Water, Glycerin, Dipropylene Glycol, Propanediol, 1,2-Hexanediol, Alcohol, Phenoxyethanol, Sodium Hyaluronate, Ethylhexylglycerin, Disodium EDTA, Disodium EDTA, Polysorbate 60, Hydroxyacetophenone, Carbomer, Tromethamine, Butylene Glycol, Brassica Oleracea Italica (Broccoli) Sprout Extract, Camellia Oleifera Leaf Extract, Eugenia Caryophyllus (Clove) Bud Extract, Magnolia Liliflora Flower Extract, Triticum Vulgare (Wheat) Sprout Extract, Glycine Soja (Soybean) Sprout Extract, Sophora Japonica Flower Extract, Allantoin, Citrus Aurantium Dulcis (Orange) Oil, Ethylhexylglycerin, Theobroma Cacao (Cocoa) Extract, Dextrin, Ecklonia cava Extract, Citrus Limon (Lemon) Peel Oil, Lavandula Angustifolia (Lavender) Oil
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
UNIWELL NATURAL TONER
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71502-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2.4 mg in 120 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.048 mg in 120 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPANEDIOL (UNII: 5965N8W85T) DIPROPYLENE GLYCOL (UNII: E107L85C40) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) ALCOHOL (UNII: 3K9958V90M) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) POLYSORBATE 60 (UNII: CAL22UVI4M) TROMETHAMINE (UNII: 023C2WHX2V) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BROCCOLI SPROUT (UNII: 128UH9LOAE) CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) CLOVE (UNII: K48IKT5321) MAGNOLIA LILIIFLORA FLOWER (UNII: SVM28292LH) WHEAT SPROUT (UNII: 3K32950CI0) SOYBEAN (UNII: L7HT8F1ZOD) STYPHNOLOBIUM JAPONICUM FLOWER (UNII: 644C3CSB6E) ALLANTOIN (UNII: 344S277G0Z) ORANGE OIL (UNII: AKN3KSD11B) COCOA (UNII: D9108TZ9KG) LEMON OIL (UNII: I9GRO824LL) LAVENDER OIL (UNII: ZBP1YXW0H8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71502-004-02 1 in 1 PACKAGE 06/13/2017 1 NDC:71502-004-01 120 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/13/2017 Labeler - uniwell LTD (694646565) Registrant - uniwell LTD (694646565) Establishment Name Address ID/FEI Business Operations Cosmecca Korea Co., Ltd. 688830827 manufacture(71502-004)
