Label: DPC DUAL MASTER VITAMIN C- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71673-0005-1 - Packager: MSCO
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated August 23, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Prunus Mume Flower Water
Hyaluronic Acid
Butylene Glycol
Water
Theanine
Milk Lipids
Glutathione
Hydrogenated Lecithin
Ceramide NP
1,2-Hexanediol
Glycerin
Panthenol
Propanediol
Benzyl Glycol
Ethylhexylglycerin
Raspberry Ketone
Hydrolyzed Hyaluronic Acid
Sodium Hyaluronate
Sodium Hyaluronate Crosspolymer
Lactococcus Ferment Lysate
Sodium Benzoate
Hydrogenated Lecithin
Polyglycerin-3
PCA
PEG-240/HDI Copolymer Bis-Decyltetradeceth-20 Ether
Malus Domestica Fruit Cell Culture Extract
Caprylyl Glycol
Tropolone
Octyldodeceth-16
Arginine
Sodium Acetylated Hyaluronate
Hydrolyzed Glycosaminoglycans
Citric Acid
Tremella Fuciformis Polysaccharide
Tuber Melanosporum Extract
Astragalus Membranaceus Root Extract
Rhizobian Gum
Copper PCA
Dipotassium Glycyrrhizate
Betaine
Acetyl Hexapeptide-8
PVP
Fullerenes
Fragrance - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DPC DUAL MASTER VITAMIN C
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71673-0005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71673-0005-1 40 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/23/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/23/2017 Labeler - MSCO (689039838) Registrant - MSCO (689039838) Establishment Name Address ID/FEI Business Operations MSCO 689039838 label(71673-0005) Establishment Name Address ID/FEI Business Operations ATEC Co., Ltd. 689276681 manufacture(71673-0005)
