FUNEES- sodium hyaluronate 
DS TECH 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.

----------

Drug Facts

Sodium hyaluronate

- roller

Water
Human Fibroblast Conditioned Media
1,2-Hexanediol
Niacinamide
Sodium Hyaluronate
sh-Pentapeptide-19
sh-Octapeptide-4
Leontopodium Alpinum Callus Culture Extract
Ethylhexylglycerin
Glutathione
Galloyl Pentapeptide-33
Glycine
Glutamine
Isoleucine
Leucine
Methionine
Phenylalanine
Serine
Threonine
Tryptophan
Valine
Folic Acid
Riboflavin
Thiamine HCl
Calcium Chloride
Magnesium Sulfate
Potassium Chloride
Sodium Pyruvate
Cysteine
Arginine
Lysine
Proline
Adenosine
Glycosyl Trehalose
Hydrogenated Starch Hydrolysate
Tromethamine
Citric Acid
Hydrolyzed F-Fucoidan

- patch

Water
Acetyl hexapeptide-8 Water
Caprylyl glycol
Acetyl hexapeptide-8
Sodium hyaluronate
Cellulose gum
Lactose
Glycerin
Marigold Extract HD Water
Calendula officinalis flower extract
1,2-Hexanediol
Licorice Extract HD Water
Glycyrrhiza uralensis (licorice) root extract
1,2-Hexanediol
GH-815 Propanediol
Caprylyl glycol
Ethylhexyl glycerin
Madecassoside

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

keep out of reach of the children

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)

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.

for topical use only

label

FUNEES 
sodium hyaluronate kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72910-0004
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72910-0004-11 in 1 BOX; Type 0: Not a Combination Product07/21/2019
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 14 PATCH 180 mL
Part 21 BOTTLE, GLASS 3.3 mL
Part 1 of 2
FUNEES 
sodium hyaluronate patch
Product Information
Item Code (Source)NDC:72910-0005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM6.14 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72910-0005-24 in 1 POUCH
1NDC:72910-0005-145 mL in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/26/2019
Part 2 of 2
AMPLE 
sodium hyaluronate liquid
Product Information
Item Code (Source)NDC:72910-0006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.8 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ADENOSINE (UNII: K72T3FS567)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72910-0006-24 in 1 BOX
1NDC:72910-0006-13.3 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/26/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/21/2019
Labeler - DS TECH CO., LTD (688510094)
Registrant - DS TECH CO., LTD (688510094)
Establishment
NameAddressID/FEIBusiness Operations
DS TECH CO., LTD688510094manufacture(72910-0004) , label(72910-0004)

Revised: 8/2019
Document Id: 8f1e2563-eeda-4102-e053-2a95a90a120a
Set id: 8e9bb49a-8cba-4390-e053-2a95a90a4e0e
Version: 2
Effective Time: 20190802
 
DS TECH CO., LTD