PURE SHINE VANILLA MAKEUP BASE 01 VANILLA GREEN by NATURE REPUBLIC CO., LTD. / Cosmecca Korea Co., Ltd.

PURE SHINE VANILLA MAKEUP BASE 01 VANILLA GREEN by

Drug Labeling and Warnings

PURE SHINE VANILLA MAKEUP BASE 01 VANILLA GREEN by is a Otc medication manufactured, distributed, or labeled by NATURE REPUBLIC CO., LTD., Cosmecca Korea Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURE SHINE VANILLA MAKEUP BASE 01 VANILLA GREEN- titanium dioxide, octinoxate cream 
NATURE REPUBLIC CO., LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ACTIVE INGREDIENT

ACTIVE INGREDIENT: Titanium Dioxide (CI 77891) 5.03%, Ethylhexyl Methoxycinnamate 2%

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Water,Cyclopentasiloxane,Phenyl Trimethicone,Butylene Glycol,Titanium Dioxide (CI 77891),Cyclohexasiloxane,4-Methylbenzylidene Camphor,Glycerin,Ethylhexyl Methoxycinnamate,Sodium Chloride,Cetyl PEG/PPG-10/1 Dimethicone,Polyglyceryl-4 Isostearate,Sorbitan Isostearate,Hexyl Laurate,Dimethicone,Disteardimonium Hectorite,Sorbitan Olivate,Dimethicone/Vinyl Dimethicone Crosspolymer,Beeswax,Butylene Glycol Dicaprylate/Dicaprate,Calcium Stearate,Ozokerite,Tocopheryl Acetate,Propylene Carbonate,Propylparaben,Methylparaben,Fragrance,Quaternium-18 Bentonite,Disodium EDTA,CI 77491,Triethanolamine,Alcohol,Silica,Vanilla Planifolia Fruit Extract,Phenoxyethanol,Sodium Hyaluronate,Ethylhexylglycerin

PURPOSE

PURPOSE: Sunscreen

WARNINGS

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

DESCRIPTION

Indications & Usage: Makeup base that evens out the skin tone.

Dosage & Administration: Apply an adequate amount to skin using either hand or puff.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PURE SHINE VANILLA MAKEUP BASE 01 VANILLA GREEN 
titanium dioxide, octinoxate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-460
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	Titanium Dioxide	1.76 g  in 35 g
Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	Octinoxate	0.70 g  in 35 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Phenyl Trimethicone (UNII: DR0K5NOJ4R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-460-01	35 g in 1 TUBE; Type 0: Not a Combination Product	05/01/2016	11/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	05/01/2016	11/01/2019

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

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

Establishment
Name	Address	ID/FEI	Business Operations
NATURE REPUBLIC CO., LTD.		631172020	manufacture(51346-460)

Revised: 2/2020

Document Id: fe7d4fb7-fb47-4d84-92c8-b117412dea3b

34390-5

Set id: 59ae9de0-a3cb-45ba-bfac-13b0d1914ee5

Version: 2

Effective Time: 20200219

 

NATURE REPUBLIC CO., LTD.