Label: DPC AURA BOOSTER MASK- niacinamide liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 71673-0001-1 - 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 17, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Glycerin
Butylene Glycol
Sodium Hyaluronate
1,2-Hexanediol
Allantoin
Dipotassium Glycyrrhizate
Trehalose
Hydroxyethylcellulose
Carbomer
PEG-60 Hydrogenated Castor Oil
Glyceryl Acrylate/Acrylic Acid Copolymer
Propylene Glycol
PVM/MA Copolymer
Panthenol
Diamond powder
Simmondsia Chinensis (Jojoba) Seed Oil
Anthemis Nobilis Flower Extract
Jasminum Officinale (Jasmine) Flower Water
Lilium Tigrinum Extract
Arnica Montana Flower Extract
Arginine
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
Citrus Grandis (Grapefruit) Seed Extract
Acorus Calamus Root Extract
Perilla Ocymoides Leaf Extract
Fragrance - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DPC AURA BOOSTER MASK
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71673-0001 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:71673-0001-1 5 in 1 PACKAGE 07/01/2017 1 25 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(71673-0001) Establishment Name Address ID/FEI Business Operations CNF CO.,LTD. 689852175 manufacture(71673-0001)