DPC Whitening Booster Mask

Manufacturer
MSCO | CNF CO.,LTD.
Effective date
2017-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:15

Label at a glance#

ProductDPC Whitening Booster Mask
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

NIACINAMIDE

INACTIVE INGREDIENT SECTION

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

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

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71673-0003-12020-01-31C16284748780-19d75b9d0-08f2-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71673-0003-1DPC Whitening Booster Mask20 g in 1 POUCHLIQUID201
71673-0003-1DPC Whitening Booster Mask5 in 1 PACKAGELIQUID51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71673-0003DPC WHITENING BOOSTER MASK (NIACINAMIDE) LIQUID [MSCO]1Legacy NDC, 2 package rows20170818_5700e699-8791-03ed-e054-00144ff8d46c.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71673-000371673-0003-1

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5700e699-8792-03ed-e054-00144ff8d46c5700e699-8791-03ed-e054-00144ff8d46c2017-08-18WarningsExact identifier
spl id: 5700e699-8792-03ed-e054-00144ff8d46c
spl set id: 5700e699-8791-03ed-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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