DIAPIA ADL EVER-CURECREAM- niacinamide, adenosine cream

DIAPIA ADL EVER-CURECREAM by

Drug Labeling and Warnings

DIAPIA ADL EVER-CURECREAM 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, Adenosine

INACTIVE INGREDIENT

Water, Glycerin, Centella Asiatica Extract, Hydrogenated Polydecene, 1,2-Hexanediol, Butylene Glycol, Cetearyl Alcohol, Polyacrylate-13, Polyisobutene, Polysorbate 20, Polysorbate 60, C13-14 Isoparaffin, Dimethicone, Sodium Polyacrylate, Simmondsia Chinensis (Jojoba) Seed Oil, Olea Europaea (Olive) Fruit Oil, Helianthus Annuus (Sunflower) Seed Oil, Betaine, Macadamia Ternifolia Seed Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Phenoxyethanol, Xanthan Gum, Triethanolamine, Disodium EDTA, Curcuma Longa (Turmeric) Root Powder, Curcuma Longa (Turmeric) Root Extract, Portulaca Oleracea Extract

PURPOSE

Brightening & Anti-wrinkle care, Soothing, Moisturizing, Relieving itching skin

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Put the appropriate amount onto face and gently massage until fully 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 ADL EVER-CURECREAM 
niacinamide, adenosine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71857-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.04 g  in 100 mL
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: 71857-0010-1	30 mL in 1 BOTTLE; 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(71857-0010) , label(71857-0010)