GINSENG ROYAL SILK by NATURE REPUBLIC CO., LTD.

GINSENG ROYAL SILK by

Drug Labeling and Warnings

GINSENG ROYAL SILK by is a Otc medication manufactured, distributed, or labeled by NATURE REPUBLIC CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GINSENG ROYAL SILK- niacinamide emulsion 
NATURE REPUBLIC CO., LTD.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENT

ACTIVE INGREDIENTS: NIACINAMIDE (2.00%)

INACTIVE INGREDIENT

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,ADENOSINE,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

PURPOSE: Skin Protectant

CAUTIONS

CAUTIONS: 1. For external use only 2. Avoid contact with eyes and mouth 3. Discontinue use if signs of irritation or rashes appear 4. Keep out of reach of children 5. Replace the cap after use

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

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

DOSAGE & ADMINISTRATION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GINSENG ROYAL SILK 
niacinamide emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-345
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2.4 mg  in 120 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-345-01	120 mL in 1 CARTON; Type 0: Not a Combination Product	09/01/2015	11/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/01/2015	11/01/2019

Labeler - NATURE REPUBLIC CO., LTD. (631172020)

Registrant - NATURE REPUBLIC CO., LTD. (631172020)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmax, Inc.		689049693	manufacture(51346-345)

Revised: 1/2020

Document Id: b9e2746e-0752-499d-8cf4-78a7d7ad519e

34390-5

Set id: 7d536b89-d954-49a0-ba1f-a7f93e3bad17

Version: 2

Effective Time: 20200111

 

NATURE REPUBLIC CO., LTD.