FUNEES- sodium hyaluronate patch

FUNEES by

Drug Labeling and Warnings

FUNEES by is a Otc medication manufactured, distributed, or labeled by DS TECH CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium hyaluronate

INACTIVE INGREDIENT

Water
Caprylyl glycol
Acetyl hexapeptide-8

Cellulose gum
Lactose
Glycerin

Calendula officinalis flower extract
1,2-Hexanediol

Glycyrrhiza uralensis (licorice) root extract
Propanediol
Ethylhexyl glycerin
Madecassoside

PURPOSE

DMS (Dissolving Micro Structure) Technology Microchip gives minute skin stimulation to help skin concentrate and absorb active ingredients

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

spread water soluble cosmetics all over your face before using

open one sterilized micro chip roller for use

press the left pushbutton of the dedicated roller handle to insert a micro chip roller

gently rolls massages along the fact surface from inside to outside

use only until you feel no stimulation from the micro chip

after using, apply cosmetics evenly across face

after using, press the roller handle depressor to discard the micro chip roller (the micro chip roller is disposable)

dedicated roller handle keeps it clean with a continous use product

(this product is recommended to use one every 2 to 3 days)

WARNINGS

Use it for your own use only.

For external use only.

Discontinue use if adverse reaction occurs.

Contact a physician if symptoms persist.

Store at room temperature

.Do not reuse it as a disposable product.

Please use it immediately after opening.

DOSAGE & ADMINISTRATION

for topical use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FUNEES 
sodium hyaluronate patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72910-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	6.14 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72910-0003-1	68 g in 1 PATCH; Type 0: Not a Combination Product	07/21/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/21/2019

Labeler - DS TECH CO., LTD (688510094)

Registrant - DS TECH CO., LTD (688510094)

Establishment
Name	Address	ID/FEI	Business Operations
DS TECH CO., LTD		688510094	manufacture(72910-0003) , label(72910-0003)