THE SKINHOUSE VITA SNAIL FIRST ESSENSE- niacinamide, adenosine liquid 
NOKSIBCHO cosmetic Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

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

Image of carton

THE SKINHOUSE VITA SNAIL FIRST ESSENSE 
niacinamide, adenosine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73590-0082
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE3.0 g  in 150 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.06 g  in 150 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73590-0082-21 in 1 CARTON07/01/2021
1NDC:73590-0082-1150 mL in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/01/2021
Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175)
Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175)
Establishment
NameAddressID/FEIBusiness Operations
NOKSIBCHO cosmetic Co., Ltd.690182175manufacture(73590-0082)

Revised: 7/2021
Document Id: 7dc9ae24-7853-481b-a600-528db0b1d23a
Set id: 20fcfd5c-7645-453a-a761-d355b0f1efc6
Version: 1
Effective Time: 20210715
 
NOKSIBCHO cosmetic Co., Ltd.