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DPC Aura Booster Mask

Medically reviewed on August 17, 2017

Dosage form: liquid
Ingredients: NIACINAMIDE 2g in 100g
Labeler: MSCO
NDC Code: 71673-0001

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 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


DPC AURA BOOSTER MASK 
niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71673-0001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (NIACINAMIDE) NIACINAMIDE2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN 
WATER 
HYALURONATE SODIUM 
GLYCERIN 
Packaging
#Item CodePackage Description
1NDC:71673-0001-15 POUCH in 1 PACKAGE
125 g in 1 POUCH
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/FEIOperations
MSCO689039838label(71673-0001)
Establishment
NameAddressID/FEIOperations
CNF CO.,LTD.689852175manufacture(71673-0001)

 
MSCO

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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