FDA.reportPublic FDA data

ROA Cytomedy Cell Pure 2500 Ampoule

Manufacturer
Beautee Collagen Co., Ltd. | EYESOME. Co.,Ltd.
Effective date
2019-02-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:31:07

Label at a glance#

ProductROA Cytomedy Cell Pure 2500 Ampoule
Active ingredientNIACINAMIDE, ADENOSINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Niacinamide 2.00%

Adenosine 0.04%

OTC - PURPOSE SECTION

Brightening

Wrinkle Improvement

INDICATIONS & USAGE SECTION

Helps wrinkle improvement and brightening

DOSAGE & ADMINISTRATION SECTION

Mix a drop of this Ampoule into your facial moisturizer, then apply gently onto your face and massage until absorbed.

WARNINGS SECTION

For external use only.
Do not use on damaged or broken skin.Stop using and ask a doctor if rash occurs.
When using this product, keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT SECTION

Water, Hydrolyzed Collagen, Dipropylene Glycol, Betaine, Alcohol, Glycerin, 1,2-Hexanediol, PEG-40 Hydrogenated Castor Oil, Glycosyl Trehalose, Hydrogenated Starch Hydrolysate, Phenoxyethanol, PPG-26-Buteth-26, PEG-32, Gluconolactone, Allantoin, PEG-8, Ammonium Acryloyldimethyltaurate/VP Copolymer, Xanthan Gum, Sodium Hyaluronate, Disodium EDTA, Beta-Glucan, Caprylyl Glycol, Sodium Polyacrylate, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72437-00172437-001-01, 72437-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIPROPYLENE GLYCOLE107L85C40IACT
BETAINE3SCV180C9WIACT
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
BEMISIOSE76B4LOB2YCIACT
HYDROGENATED STARCH HYDROLYSATE27F77DSJ5VIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PPG-26-BUTETH-262II1K6TZ4PIACT
POLYETHYLENE GLYCOL 15001212Z7S33AIACT
GLUCONOLACTONEWQ29KQ9POTIACT
ALLANTOIN344S277G0ZIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
XANTHAN GUMTTV12P4NEEIACT
HYALURONATE SODIUMYSE9PPT4THIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CURDLAN6930DL209RIACT
CAPRYLYL GLYCOL00YIU5438UIACT
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
NIACINAMIDE25X51I8RD4ACTIB
ADENOSINEK72T3FS567ACTIB
WATER059QF0KO0RIACT
MARINE COLLAGEN, SOLUBLE8JC99XGU4WIACT

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
c478ec01-9629-15a6-e053-2995a90a7c0144e2fd79-84c8-4ef8-a26e-4b250fad51cb2021-06-11WarningsExact identifier
spl set id: 44e2fd79-84c8-4ef8-a26e-4b250fad51cb

Reported adverse events (FAERS/openFDA)#

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