CELLEXOSOME HE HR- niacinamide liquid

CellExosome HE HR by

Drug Labeling and Warnings

CellExosome HE HR 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: Niacinamide 3.0%

INACTIVE INGREDIENT

Inactive ingredients:

[Powder] HUMAN ADIPOSE DERIVED STEM CELL CONDITIONED MEDIA, Asparagus Officinalis Extract
[Solvent] Water, Panthenol, 1,2-Hexanediol, Hydroxyacetophenone, Sodium Hyaluronate

PURPOSE

Purpose: Hair elasticity

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:

Improves effects of hair elasticity.

Directions

Directions:

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CELLEXOSOME HE HR 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62041-310
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	Niacinamide	0.18 g  in 6 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Panthenol (UNII: WV9CM0O67Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62041-310-02	1 in 1 CARTON	02/01/2020
1	NDC: 62041-310-01	6 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(62041-310)