ORGANIC NIGHT REPAIR AMPOULE- niacinamide, adenosine cream 
yeojaya

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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ACTIVE INGREDIENT

Active ingredients: Niacinamide 2.5%, Adenosine 0.1%

INACTIVE INGREDIENT

Inactive ingredients:

Aloe Barbadensis Leaf Water, Sodium Hyaluronate, Butylene Glycol, Glycerin, Palmitoyl Pentapeptide-4, Glyceryl Glucoside, 1,2-Hexanediol, rh-Oligopeptide-1, Trehalose, Polysorbate 20, Sorbitol, Arginine, Petroselinum Sativum (Parsley) Extract, Cucumis Sativus (Cucumber) Fruit Extract, Althaea Officinalis Root Extract, Centaurea Cyanus Flower Extract, Citrus Limon (Lemon) Fruit Extract, Red Ginseng Extract, Calendula Officinalis Flower Extract, Caprylyl Glycol, Illicium Verum (Anise) Fruit Extract, Pearl Powder, Fragrance, Ceramide NP

PURPOSE

Purpose: Skin Brightening, Anti wrinkle

WARNINGS

Warnings:

- For external use only

- Avoid contact with eyes.

- Discontinue use if signs of irritation or rashes appear.

- Replace the cap after use.

- Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

Uses:

- Helps improve skin brightening

- Helps improve Anti wrinkle

Directions

Directions:

- After cleansing, apply appropriate amount on skin and absorb gently into skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

ORGANIC NIGHT REPAIR AMPOULE 
niacinamide, adenosine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69142-020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide1.12 g  in 45 mL
Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.04 g  in 45 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69142-020-021 in 1 CARTON08/01/2018
1NDC:69142-020-0145 mL in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/01/2018
Labeler - yeojaya (688735127)
Registrant - yeojaya (688735127)
Establishment
NameAddressID/FEIBusiness Operations
yeojaya688735127manufacture(69142-020)

Revised: 9/2018
Document Id: 31f16dde-d692-4f45-83fc-ffd864a0073a
Set id: 59dc99a2-659b-4b65-8e21-24f62aa60a03
Version: 1
Effective Time: 20180917
 
yeojaya