NGF 574H HAIR- panthenol solution

NGF 574H HAIR by

Drug Labeling and Warnings

NGF 574H HAIR by is a Otc medication manufactured, distributed, or labeled by Celino Inc., Interkos Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Panthenol 1.00%

INACTIVE INGREDIENTS

Water, Human Cord Blood Cell Conditioned Media, Propanediol, Hydroxypropyl Cyclodextrin, 1,2-Hexanediol,Sodium Chloride, Butylene Glycol, Cellulose Gum, Glyceryl Caprylate, Ethylhexylglycerin, Sodium Hyaluronate

PURPOSE

Hair growth

WARNINGS

1. Stop using this product and see a dermatologist, if skin swelling, itching or skin rashes appear after using this product or by exposure to sun light 2. Refrain from applying the product on wounded skin area 3. Cautions during storage and handling a) keep out of reach from infants and children b) store away from direct sunlight 4. Wash out immediately when in contact with eyes 5. For external use only

KEEP OUT OF REACH OF CHILDREN

keep out of reach from infants and children

Uses

A hair solution containing high concentration of primed, human cord blood cell conditioned media whose performance in haircare is proved by clinical study
+ Safety and efficacy proved in clinical trials
+ Patent granted (Pat# 10-1836029)

Directions

1. Use steadily for more than 4 weeks.
2. Apply solution close to the scalp that needs care.

QUESTIONS

080-750-1800 www.celonia.co.kr

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NGF 574H HAIR 
panthenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73655-130
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Panthenol (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	Panthenol	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Propanediol (UNII: 5965N8W85T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73655-130-02	5 in 1 CARTON	10/01/2021
1	NDC: 73655-130-01	3 mL in 1 VIAL; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/01/2021

Labeler - Celino Inc. (695738827)

Registrant - Celino Inc. (695738827)

Establishment
Name	Address	ID/FEI	Business Operations
Interkos Co.,Ltd.		689850314	manufacture(73655-130)