FDA.reportPublic FDA data

DIAPIA HA Aqua Shining Mask

Manufacturer
BSG H & B Co., Ltd.
Effective date
2021-12-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:45:36

Label at a glance#

ProductDIAPIA HA Aqua Shining Mask
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Niacinamide

INACTIVE INGREDIENT SECTION

Water
Methylpropanediol
Glycerin
Water
Glycereth-26
Butylene Glycol
PEG/PPG-17/6 Copolymer
Water
Hydroxyethyl Urea
1,2-Hexanediol
Phenoxyethanol
Triethanolamine
Water
Water
Butylene Glycol
Sodium Hyaluronate
Phenoxyethanol
Saccharide Isomerate
Water
Sodium Citrate
Citric Acid
PPG-26-Buteth-26
PEG-40 Hydrogenated Castor Oil
Water
Dipotassium Glycyrrhizate
Carbomer
Allantoin
Hydroxyethylcellulose
Sodium Nitrate
Xanthan Gum
Water
Butylene Glycol
Vaccinium Angustifolium (Blueberry) Fruit Extract
Rubus Idaeus (Raspberry) Fruit Extract
Rubus Fruticosus (Blackberry) Fruit Extract
Euterpe Oleracea Fruit Extract
Fragaria Chiloensis (Strawberry) Fruit Extract
Phenoxyethanol
Water
Aloe Barbadensis Leaf Extract
Butylene Glycol
Phenoxyethanol
Water
Camellia Sinensis Leaf Extract
Butylene Glycol
Phenoxyethanol
Tetrasodium EDTA
Parfum
Polyglutamic Acid
Water

OTC - PURPOSE SECTION

Brightening, anti wrinkle care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

after cleansing trim the skin with toner, take out the mask sheet, unfuld and then remove the films

put the upper and lower mask sheets tightly on face according to the shape

after taking a comfortable rest for 10-20 minutes, remove the mask and lightly pat the remaining cream for better absorption

WARNINGS SECTION

1.Keep out of reach of children.

2.Store in a cool, dry place and avoid direct sunlight.

3.If abnormal symptoms occur after use, stop use and consult with a skin specialist.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71857-0019-22023-01-30C16284748780-1f386c649-ed93-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71857-0019-1DIAPIA HA Aqua Shining Mask24 mL in 1 POUCHLIQUID241
71857-0019-2DIAPIA HA Aqua Shining Mask5 in 1 BOXLIQUID51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71857-0019DIAPIA HA AQUA SHINING MASK (NIACINAMIDE) LIQUID [BSG H & B CO., LTD.]1Legacy NDC, 2 package rows20211212_d2c85f77-3c96-5b61-e053-2a95a90aa8b3.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71857-001971857-0019-1, 71857-0019-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4ACTIB

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
d2c85fbd-801c-7ec4-e053-2a95a90a8acfd2c85f77-3c96-5b61-e053-2a95a90aa8b32021-12-10WarningsExact identifier
spl id: d2c85fbd-801c-7ec4-e053-2a95a90a8acf
spl set id: d2c85f77-3c96-5b61-e053-2a95a90aa8b3

Reported adverse events (FAERS/openFDA)#

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