DIAPIA HA AQUA SHINING MASK- niacinamide liquid

DIAPIA HA AQUA SHINING MASK by

Drug Labeling and Warnings

DIAPIA HA AQUA SHINING MASK by is a Otc medication manufactured, distributed, or labeled by BSG H & B Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Niacinamide

INACTIVE INGREDIENT

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

PURPOSE

Brightening, Moisturizing, Softening, Soothing

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

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

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

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIAPIA HA AQUA SHINING MASK 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71857-0013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71857-0013-1	24 mL in 1 POUCH; Type 0: Not a Combination Product	10/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/30/2020

Labeler - BSG H & B Co., Ltd. (694252895)

Registrant - BSG H & B Co., Ltd. (694252895)

Establishment
Name	Address	ID/FEI	Business Operations
BSG H & B Co., Ltd.		694252895	manufacture(71857-0013) , label(71857-0013)