DPC AURA BOOSTER MASK- niacinamide liquid

DPC Aura Booster Mask by

Drug Labeling and Warnings

DPC Aura Booster Mask by is a Otc medication manufactured, distributed, or labeled by MSCO, CNF CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

NIACINAMIDE

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

Skin Protectant - Intensive Whitening

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

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.

WARNINGS

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

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DPC AURA BOOSTER MASK 
niacinamide liquid

Product 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)