DPC AURA BOOSTER MASK- niacinamide liquid 
MSCO

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.

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Drug Facts

NIACINAMIDE

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

Skin Protectant - Intensive Whitening

keep out of reach of the children

1. After cleansing wipe water and apply skin lotion on face.
2. Apply the mask evenly over the face for 10-20 minutes and remove.
3. Pad the left over residue lightly to absorb.

For external use only.
Avoid contact with eyes. Not for human consumption.
Discontinue use if irritation occurs.
If irritation persists, consult a physician.

for external use only


1

DPC AURA BOOSTER MASK 
niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71673-0001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN (UNII: 344S277G0Z)  
WATER (UNII: 059QF0KO0R)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71673-0001-15 in 1 PACKAGE07/01/2017
125 g in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/01/2017
Labeler - MSCO (689039838)
Registrant - MSCO (689039838)
Establishment
NameAddressID/FEIBusiness Operations
MSCO689039838label(71673-0001)
Establishment
NameAddressID/FEIBusiness Operations
CNF CO.,LTD.689852175manufacture(71673-0001)

Revised: 8/2017
Document Id: 56ff4b98-b530-39cb-e054-00144ff8d46c
Set id: 56ff4b98-b527-39cb-e054-00144ff8d46c
Version: 1
Effective Time: 20170817
 
MSCO