DPC Whitening Booster Mask: Package Insert and Label Information

DPC WHITENING 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.

NIACINAMIDE

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

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

DPC WHITENING BOOSTER MASK niacinamide liquid

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71673-0003 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (NIACINAMIDE) NIACINAMIDE 2 g in 100 g

Inactive Ingredients Ingredient Name Strength ALLANTOIN WATER HYALURONATE SODIUM GLYCERIN

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:71673-0003-1 5 POUCH in 1 PACKAGE contains a POUCH 1 20 g in 1 POUCH This package is contained within the PACKAGE (71673-0003-1)

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	Operations
MSCO		689039838	label (71673-0003)

Establishment
Name	Address	ID/FEI	Operations
CNF CO.,LTD.		689852175	manufacture (71673-0003)

Revised: 08/2017 MSCO