DPC WHITENING BOOSTER MASK- niacinamide liquid

DPC Whitening Booster Mask by

Drug Labeling and Warnings

DPC Whitening 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
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

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 WHITENING BOOSTER MASK 
niacinamide liquid

Product 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)