EASYDEW DW EGF DERMA NEEDLE 3000 SHOT- nepidermin solution
DN Company Co.,Ltd.

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: 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

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

Image of carton

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

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:60565-260-02	4 in 1 CARTON	03/01/2018	12/01/2021
1	NDC:60565-260-01	45 mg in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		03/01/2018	12/01/2021

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

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

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

Revised: 11/2022

Document Id: b6d503a3-90c9-488b-b08a-e1a4271c8aaf

Set id: 5322ffb2-5236-4e59-ad56-33892c10b10c

Version: 2

Effective Time: 20221110

DN Company Co.,Ltd.