FDA.reportPublic FDA data

GINSENG ROYAL SILK 120ML

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc
Effective date
2017-01-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:20:39

Label at a glance#

ProductGINSENG ROYAL SILK 120ML
Active ingredientNIACINAMIDE, ADENOSINE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: NIACINAMIDE (2.00%), ADENOSINE (0.04%)

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: WATER,CAPRYLIC/CAPRIC TRIGLYCERIDE,C12-20 ACID PEG-8 ESTER,GLYCERIN, PENTYLENE GLYCOL,PEG-8,HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER,MICA (CI 77019),SILICA,POLYSORBATE 60,CYCLOPENTASILOXANE,TITANIUM DIOXIDE (CI 77891),PHENOXYETHANOL,CAPRYLYL GLYCOL,HYDROGENATED LECITHIN,XANTHAN GUM,TROMETHAMINE,FRAGRANCE(PARFUM),DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER,ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER,DISODIUM EDTA,CARBOMER,TOCOPHERYL ACETATE,BIOSACCHARIDE GUM-1,PANAX GINSENG ROOT EXTRACT,CYCLOHEXASILOXANE,ROYAL JELLY EXTRACT,GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER,TIN OXIDE (CI 77861),GOLD (CI 77480),1,2-HEXANEDIOL,BUTYLENE GLYCOL,YELLOW 6 (CI 15985),YELLOW 5 (CI 19140),ETHYL HEXANEDIOL,SILK AMINO ACIDS,ETHYLHEXYLGLYCERIN

PURPOSE

OTC - PURPOSE SECTION

Purpose: BRIGHTENING & WRINKLE IMPROVEMENT

CAUTIONS

WARNINGS SECTION

CAUTIONS: For external use only. Avoid contact with eyes and mouth. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children. Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

HOW TO USE

INDICATIONS & USAGE SECTION

HOW TO USE: After using essence, apply an appropriate amount all over the face.

HOW TO USE

DOSAGE & ADMINISTRATION SECTION

HOW TO USE: After using essence, apply an appropriate amount all over the face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-42951346-429-01, 51346-429-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4ACTIB
ADENOSINEK72T3FS567ACTIB
WATER059QF0KO0RIACT
PENTYLENE GLYCOL50C1307PZGIACT

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
f85d0537-3505-46a4-9085-79732ea770bf4beeaf6c-9f33-49f8-b381-a91179cd64e42017-01-16WarningsExact identifier
spl id: f85d0537-3505-46a4-9085-79732ea770bf
spl set id: 4beeaf6c-9f33-49f8-b381-a91179cd64e4

Reported adverse events (FAERS/openFDA)#

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