Label: FUNEES- sodium hyaluronate kit
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Contains inactivated NDC Code(s)
NDC Code(s): 72910-0004-1, 72910-0005-1, 72910-0005-2, 72910-0006-1, view more72910-0006-2 - Packager: DS TECH CO., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 Label Information
Updated August 2, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
- 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 - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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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
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FUNEES
sodium hyaluronate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72910-0004 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72910-0004-1 1 in 1 BOX; Type 0: Not a Combination Product 07/21/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 4 PATCH 180 mL Part 2 1 BOTTLE, GLASS 3.3 mL Part 1 of 2 FUNEES
sodium hyaluronate patchProduct Information Item Code (Source) NDC:72910-0005 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72910-0005-2 4 in 1 POUCH 1 NDC:72910-0005-1 45 mL in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/26/2019 Part 2 of 2 AMPLE
sodium hyaluronate liquidProduct Information Item Code (Source) NDC:72910-0006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 0.8 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ADENOSINE (UNII: K72T3FS567) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72910-0006-2 4 in 1 BOX 1 NDC:72910-0006-1 3.3 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/26/2019 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(72910-0004) , label(72910-0004)