EASYDEW DW EGF DERMA NEEDLE 3000 SHOT- nepidermin solution

EASYDEW DW EGF Derma Needle 3000 Shot by

Drug Labeling and Warnings

EASYDEW DW EGF Derma Needle 3000 Shot by is a Otc medication manufactured, distributed, or labeled by DN Company Co.,Ltd., Small Lab Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Nepidermin 0.0001 % (1ppm)

INACTIVE INGREDIENT

Inactive ingredients:

Sodium hyaluronate, Algin, Lactose, Glycerin, Simmondsia Chinensis(jojoba) See Oil, Propanediol, Caprylyl Glycol, Madecassoside, Ethylhexyglycerin, Acetyl hexapeptide-8

PURPOSE

Purpose: Wrinkle improvement

WARNINGS

Warnings:

For external use only. Keep out of reach of children. Do not use in wounds, eczemas or dermatitis. If you develop rash, itchiness or irritation, discontinue the use. Keep in a cool and dry place. Do not give strong impacts or drop the product. Use immediately after opening and do not re-use the Needle since it is a disposable product.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

Uses:

The Needle Puff containing Nepidermin (DW-EGF™) helps to deliver nutrients to the skin efficiently.

Directions

Directions:

Combine sterilized Derma Needle 3000 Shot with the Derma Needle 3000 Shot Roller. Apply half of the Derma Oneshot Ampoule on the face and proceed with massaging thoroughly(5~10 minutes). Apply the rest of the ampoule on the face and remove Derma Needle 3000 Shot and dispose after done using.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EASYDEW DW EGF DERMA NEEDLE 3000 SHOT 
nepidermin solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60565-260
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Nepidermin (UNII: TZK30RF92W) (HUMAN EPIDERMAL GROWTH FACTOR - UNII:TZK30RF92W)	Nepidermin	0.000045 mg  in 45 mg

Inactive Ingredients
Ingredient Name	Strength
Glycerin (UNII: PDC6A3C0OX)
Propanediol (UNII: 5965N8W85T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60565-260-02	4 in 1 CARTON	03/01/2018
1	NDC: 60565-260-01	45 mg 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		03/01/2018

Labeler - DN Company Co.,Ltd. (688369859)

Registrant - DN Company Co.,Ltd. (688369859)

Establishment
Name	Address	ID/FEI	Business Operations
Small Lab Co., Ltd.		688438425	manufacture(60565-260)