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
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

PURPOSE

Brightening, anti wrinkle care

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

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

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: 71857-0019
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: 71857-0019-2	5 in 1 BOX	12/01/2021
1	NDC: 71857-0019-1	24 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/01/2021

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	label(71857-0019) , manufacture(71857-0019)