FDA.reportPublic FDA data

DERMAFROM LACTO GREEN AMPOULE

Manufacturer
Rea Company | YEGREENA CO., LTD.
Effective date
2022-10-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:50:37

Label at a glance#

ProductDERMAFROM LACTO GREEN AMPOULE
Active ingredientNiacinamide, Adenosine
Label structure10 sections

Dosage and administration

■ Take an appropriate amount, spread it over the entire face and tap it lightly

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Niacinamide 2%
Adenosine 0.04%

PURPOSE

OTC - PURPOSE SECTION

Skin Brightening
Anti-Wrinkle

Use(s)

INDICATIONS & USAGE SECTION

■ To moisturize the skin
■ To whitening wrinkle improvement
■ For the management of acne

Warnings

WARNINGS SECTION

1) Consult with a specialist if there are any abnormal symptoms or side effects, such as red spots, swelling or itching etc
2) Do not use in areas with wounds.
3) Avoid contact with eyes
4) Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Take an appropriate amount, spread it over the entire face and tap it lightly

Other Information

OTHER SAFETY INFORMATION

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

Questions

OTC - QUESTIONS SECTION

■ +82-2-2257-8882
■ jaunmall.com

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Alcohol, Allantoin, Panthenol, Betaine, Aloe Barbadensis Leaf Juice Powder, Streptococcus Thermophilus Ferment, 1, 2-Hexanediol, Sodium Hyaluronate, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Tremella Fuciformis (mushroom) Extract, Glycerin, Phenoxyethanol, Ethylhexylglycerin, Portulaca Oleracea Extract, Hydrolyzed Collagen, Acetyl Hexapeptide-8, Copper tripeptide-1, Palmitoyl pentapeptide-4, Tripeptide-1, Palmitoyl tripeptide-1, Hexapeptide-9, Nonapeptide-7, Caprylyl Glycol, Carbomer, PEG-60 Hydrogenated Castor Oil, Fragrance, Hexyl Cinnamal, Disodium EDTA, CL 42090, CL 17200

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82916-160-022024-01-31C16284748780-10191ceaa-6cb5-198a-e063-dbdaa90aec3e3d13dbe5-1fa5-4d46-bdb5-41539400670f
82916-160-022023-07-28C16284748780-10191ceaa-6cb5-198a-e063-dbdaa90aec3e3d13dbe5-1fa5-4d46-bdb5-41539400670f

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82916-16082916-160-01, 82916-160-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Niacinamide25X51I8RD4ACTIB
AdenosineK72T3FS567ACTIB
Water059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT
Alcohol3K9958V90MIACT

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
10348118-fbb7-2edb-e063-6394a90a25923d13dbe5-1fa5-4d46-bdb5-41539400670f2024-01-30WarningsExact identifier
spl set id: 3d13dbe5-1fa5-4d46-bdb5-41539400670f

Reported adverse events (FAERS/openFDA)#

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