THE SKINHOUSE VITA SNAIL FIRST ESSENSE- niacinamide, adenosine liquid

THE SKINHOUSE VITA SNAIL FIRST ESSENSE by

Drug Labeling and Warnings

THE SKINHOUSE VITA SNAIL FIRST ESSENSE by is a Otc medication manufactured, distributed, or labeled by NOKSIBCHO cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

NIACINAMIDE 2.0%
ADENOSINE 0.04%

INACTIVE INGREDIENTS

Water(Aqua), Butylene Glycol, 1,2-Hexandiol, Snail Secretion Filtrate, Galactomyces Ferment Filtrate, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Allantoin, Panthenol, Betaine, Ethylhexylglycerin, Citrus Nobilis (Mandarin Orange) Peel Extract, Cupressus Sempervirens Leaf/Stem Extract, Hedera Helix (Ivy) Leaf/Stem Extract, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Ribes Nigrum (Black Currant) Leaf Extract, Litsea Cubeba Fruit Oil, Sodium Hyaluronate, Ascorbic Acid, Vaccinium Angustifolium (Blueberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Centella Asiatica Extract, Hydrolyzed Collagen

PURPOSE

Skin Brightening
Anti wrinkle

WARNINGS

For external use only.
Avoid contact with eyes.
Keep out of reach of children.
Discontinue use if signs of irritation appear.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

Uses

■ It refreshes and smoothes skin and effectively prepares the next skin care routines.

Directions

■ Use in the morning and at night after cleansing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

THE SKINHOUSE VITA SNAIL FIRST ESSENSE 
niacinamide, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73590-0082
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	3.0 g  in 150 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.06 g  in 150 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73590-0082-2	1 in 1 CARTON	07/01/2021
1	NDC: 73590-0082-1	150 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2021

Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175)

Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175)

Establishment
Name	Address	ID/FEI	Business Operations
NOKSIBCHO cosmetic Co., Ltd.		690182175	manufacture(73590-0082)