FDA.reportPublic FDA data

DIAPIA HA AQUA SHINING MASK

Manufacturer
BSG H & B Co., Ltd.
Effective date
2020-10-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:39

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, Butylene Glycol, Glycereth-26, Glycerin, Methylpropanediol, 1,2-Hexanediol, Phenoxyethanol, Carbomer, Hydroxyethyl Urea, Triethanolamine, Dipotassium Glycyrrhizate, Allantoin, PEG/PPG-17/6 Copolymer, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Saccharide Isomerate, Xanthan Gum, Tetrasodium EDTA, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Sodium Hyaluronate, Vaccinium Angustifolium (Blueberry) Fruit Extract,

Rubus Idaeus (Raspberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Fragaria Chiloensis (Strawberry) Fruit Extract, Fragrance, Sodium Citrate, Citric Acid, Polyglutamic Acid, Hydroxyethylcellulose

OTC - PURPOSE SECTION

Brightening, Moisturizing, Softening, Soothing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Cleanse and dry face thoroughly.

Open pouch, unfold mask and apply to face.

Leave it for 10 - 20 minutes, remove the mask and tap slightly until essence

absorbed.

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
71857-0013-12022-01-28C16284748780-1d6a99b39-7e6f-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71857-0013-1DIAPIA HA AQUA SHINING MASK24 mL in 1 POUCHLIQUID241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71857-0013DIAPIA HA AQUA SHINING MASK (NIACINAMIDE) LIQUID [BSG H & B CO., LTD.]1Legacy NDC, 1 package rows20201030_b2dafe3f-8b1d-a743-e053-2995a90aef8d.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
71857-001371857-0013-1

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
b2dafb49-f806-9ec2-e053-2995a90acd8bb2dafe3f-8b1d-a743-e053-2995a90aef8d2020-10-29WarningsExact identifier
spl id: b2dafb49-f806-9ec2-e053-2995a90acd8b
spl set id: b2dafe3f-8b1d-a743-e053-2995a90aef8d

Reported adverse events (FAERS/openFDA)#

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