FDA.reportPublic FDA data

GINSENG ROYAL SILK AMPOULE

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc
Effective date
2017-01-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:20:42

Label at a glance#

ProductGINSENG ROYAL SILK AMPOULE 17mL 4ea
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, Dipropylene Glycol, Polyglycerin-3,Alcohol, Pentylene Glycol, Linum Usitatissimum (Linseed) Seed Extract,1,2-Hexanediol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Phenoxyethanol, PEG-60 Hydrogenated Castor Oil, Butylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Panax Ginseng Root Extract,Royal Jelly Extract, Octyldodeceth-16, Glyceryl Polyacrylate, Tromethamine, Polyquaternium-5, Sodium Polyacrylate, Xanthan Gum, Adenosine, Fragrance(Parfum), Gold (CI 77480), Hydrolyzed Corn Starch, Disodium EDTA, Mica (CI 77019), Titanium Dioxide (CI 77891), Sucrose, Ethyl Hexanediol, Carbomer, Iron Oxides (CI 77491), Polysorbate 20, Tin Oxide (CI 77861), Palmitoyl Tripeptide-1, Cyclohexasiloxane, Palmitoyl Tetrapeptide-7, Silk Amino Acids, Ethylhexylglycerin

PURPOSE

OTC - PURPOSE SECTION

Purpose: Brightening & Wrinkle Improvement

WARNINGS

WARNINGS SECTION

Warnings: For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. 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.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

After using toner, apply an appropriate amount on the entire face and gently pat to promote absorption into skin.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: After using toner, apply an appropriate amount on the entire face and gently pat to promote absorption into skin.

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
51346-42351346-423-01, 51346-423-02

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
Dipropylene GlycolE107L85C40IACT

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
77e733a9-a562-4595-834d-8d20b1843710fc6f4b9f-789b-4d74-8fdf-9cf768c468e62017-01-13WarningsExact identifier
spl id: 77e733a9-a562-4595-834d-8d20b1843710
spl set id: fc6f4b9f-789b-4d74-8fdf-9cf768c468e6

Reported adverse events (FAERS/openFDA)#

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