DPC Aura Booster Mask

Manufacturer: MSCO | CNF CO.,LTD.
Effective date: 2017-08-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:52:14

Label at a glance#

ProductDPC Aura Booster Mask

Active ingredientNIACINAMIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

NIACINAMIDE

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Skin Protectant - Intensive Whitening

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

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 SECTION

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 SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71673-0001-1	2020-01-31	C162847	48780-1	9d75b9d1-1083-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71673-0001-1	DPC Aura Booster Mask	5 in 1 PACKAGE	LIQUID	5		1
71673-0001-1	DPC Aura Booster Mask	25 g in 1 POUCH	LIQUID	25		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71673-0001	DPC AURA BOOSTER MASK (NIACINAMIDE) LIQUID [MSCO]	1	Legacy NDC, 2 package rows	20170818_56ff4b98-b527-39cb-e054-00144ff8d46c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

DPC Aura Booster Mask
NIACINAMIDE
ALLANTOIN
WATER
HYALURONATE SODIUM
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71673-0001	71673-0001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALLANTOIN	344S277G0Z	IACT
WATER	059QF0KO0R	IACT
HYALURONATE SODIUM	YSE9PPT4TH	IACT
NIACINAMIDE	25X51I8RD4	ACTIB
GLYCERIN	PDC6A3C0OX	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
56ff4b98-b530-39cb-e054-00144ff8d46c			56ff4b98-b527-39cb-e054-00144ff8d46c	2017-08-17	Warnings	Exact identifier spl id: 56ff4b98-b530-39cb-e054-00144ff8d46c spl set id: 56ff4b98-b527-39cb-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.