FUNEES

Manufacturer
DS TECH CO., LTD
Effective date
2019-08-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:59:58

Label at a glance#

ProductFUNEES
Active ingredientHYALURONATE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium hyaluronate

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

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 SECTION

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 SECTION

for topical use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72910-0003-12022-01-28C16284748780-1d6a99b39-9eb2-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72910-0003-1FUNEES68 g in 1 PATCHPATCH682

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72910-0003FUNEES (SODIUM HYALURONATE) PATCH [DS TECH CO., LTD]2Legacy NDC, 1 package rows20190802_8e9af06f-745b-0dfa-e053-2a95a90a8e2d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72910-000372910-0003-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONATE SODIUMYSE9PPT4THACTIB
ACETYL HEXAPEPTIDE-8L4EL31FWILIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
8f1e2563-eed1-4102-e053-2a95a90a120a8e9af06f-745b-0dfa-e053-2a95a90a8e2d2019-08-02WarningsExact identifier
spl id: 8f1e2563-eed1-4102-e053-2a95a90a120a
spl set id: 8e9af06f-745b-0dfa-e053-2a95a90a8e2d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.