Label: DPC WHITENING BOOSTER MASK- niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71673-0003-1 - Packager: MSCO
- 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 August 18, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water
Dipropylene glycol
Methylpropanediol
Alcohol
Glycerin
Sodium Hyaluronate
1,2-Hexanediol
Biosaccharide Gum-1
Boswellia Serrata Resin Extract
Butylene Glycol
Allantoin
Dipotassium Glycyrrhizate
Beta-Glucan
Hydroxyethylcellulose
Acrylates/c10-30 alkyl acrylate crosspolymer
Simmondsia Chinensis (Jojoba) Seed Oil
Citrus Limon (Lemon) Fruit Extract
Citrus Aurantium Dulcis (Orange) Fruit Water
Oryza Sativa (Rice) Extract
Citrus Aurantifolia (Lime) Fruit Extract
Citrus Paradisi (Grapefruit) Fruit Extract
Caprylic/capric Triglyceride
Hydrogenated Lecithin
Phytosteryl/octyldodecyl Lauroyl Glutamate
Ceramide NP
Polyglyceryl-10 Laurate
Polyglyceryl-10 Myristate
Arginine
Dehydroacetic acid
Chlorphenesin
Disodium EDTA
Glycyrrhiza Glabra (Licorice) Root Extract
Zingiber Officinale (Ginger) Root Extract
Schizandra Chinensis Fruit Extract
Coptis Japonica Root Extract
Camellia Sinensis Leaf Extract
Caprylyl Glycol
Fragrance - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DPC WHITENING BOOSTER MASK
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71673-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 g Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) WATER (UNII: 059QF0KO0R) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71673-0003-1 5 in 1 PACKAGE 07/01/2017 1 20 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2017 Labeler - MSCO (689039838) Registrant - MSCO (689039838) Establishment Name Address ID/FEI Business Operations MSCO 689039838 label(71673-0003) Establishment Name Address ID/FEI Business Operations CNF CO.,LTD. 689852175 manufacture(71673-0003)