CELLEXOSOME ST- adenosine liquid

CellExosome ST by

Drug Labeling and Warnings

CellExosome ST by is a Otc medication manufactured, distributed, or labeled by PROSTEMICS Co., Ltd., Prostemics Co., Ltd. Factory. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Adenosine 0.04%

INACTIVE INGREDIENT

Inactive ingredients:

[Powder] HUMAN ADIPOSE DERIVED STEM CELL CONDITIONED MEDIA, Panax Ginseng Root Extract.

[Solvent] Water, Dimethylaminoethanol Tartrate, Tromethamine, 1,2-Hexanediol, Hydroxyacetophenone, Sodium Hyaluronate

PURPOSE

Purpose: Anti wrinkle

WARNINGS

Warnings:
For external use only
1. Discontinue use if signs of irritation or rashes appear. If symptoms get worse, consult with a dermatologist. 1) In case of swelling, itching, or other side effects while or after using this product
2. Do not apply to open wounds.
3. Avoid contact with eyes.
Storage and handling
4. Replace the cap after use
5. Keep out of reach of children.
6. Avoid direct sunlight.

KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN SECTION

Uses

Uses:

Helps improve wrinkle problem

Directions

Directions:

■ Put solvent into the powder ampoule and shake gently enough to dissolve the mixture
■ Take proper amount and gently apply onto the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CELLEXOSOME ST 
adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62041-290
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	Adenosine	0.001 g  in 3 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
DEANOL BITARTRATE (UNII: D240J05W14)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62041-290-02	5 in 1 CARTON	02/01/2020
1	NDC: 62041-290-01	3 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		02/01/2020

Labeler - PROSTEMICS Co., Ltd. (689605919)

Registrant - PROSTEMICS Co., Ltd. (689605919)

Establishment
Name	Address	ID/FEI	Business Operations
Prostemics Co., Ltd. Factory		695687674	manufacture(62041-290)