FDA.reportPublic FDA data

GINSENG ROYAL SILK CAP SULE ESSENCE

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc
Effective date
2017-01-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:20:49

Label at a glance#

ProductGINSENG ROYAL SILK CAP SULE ESSENCE
Active ingredientNiacinamide, Adenosine
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Niacinamide 2.0%, Adenosine 0.04%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water,Dipropylene Glycol,PEG-8,Glycerin,Niacinamide,Linum Usitatissimum (Linseed) Seed Extract,Alcohol Denat.,Butylene Glycol,Pentylene Glycol,Polyglycerin-3,1,2-Hexanediol,Chondrus Crispus Powder,Phenoxyethanol,PEG-60 Hydrogenated Castor Oil,Ammonium Acryloyldimethyltaurate/VP Copolymer,Tromethamine,Carbomer,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Agar,Iron Oxides (CI 77491),Mica (CI 77019),Synthetic Fluorphlogopite,Titanium Dioxide (CI 77891),Panax Ginseng Root Extract,Royal Jelly Extract,Xanthan Gum,Adenosine,Fragrance(Parfum),Disodium EDTA,Gold (CI 77480),Algin,Gellan Gum,Pectin,Elaeis Guineensis (Palm) Kernel Oil,Elaeis Guineensis (Palm) Oil,Tin Oxide (CI 77861),Ethyl Hexanediol,Cyclohexasiloxane,Arginine,Sodium PCA,Silk Amino Acids,Ethylhexylglycerin

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin 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

Indications & usage: Ginseng Royal Silk Capsule Essence helps brighten skin complexion.

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-419-022021-06-25C16284748780-1ba0f9c33-2c4c-a910-e053-dadaa90a0b850568cdcd-c4ec-4603-8eda-db5c40fc5861
51346-419-022021-01-29C16284748780-1ba0f9c33-2c4c-a910-e053-dadaa90a0b850568cdcd-c4ec-4603-8eda-db5c40fc5861

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
51346-41951346-419-01, 51346-419-02

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
40c4d2b6-2dda-4cb9-b4aa-f2189238d2750568cdcd-c4ec-4603-8eda-db5c40fc58612021-06-25WarningsExact identifier
spl set id: 0568cdcd-c4ec-4603-8eda-db5c40fc5861

Reported adverse events (FAERS/openFDA)#

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