DEOPROCE UV WATERFUL CUSHION NO 13 Light Beige by Greencos Co., Ltd.

DEOPROCE UV WATERFUL CUSHION NO 13 Light Beige by

Drug Labeling and Warnings

DEOPROCE UV WATERFUL CUSHION NO 13 Light Beige by is a Otc medication manufactured, distributed, or labeled by Greencos Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DEOPROCE UV WATERFUL CUSHION NO 13 LIGHT BEIGE- titanium dioxide, octinoxate, octisalate, octocrylene powder 
Greencos 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 ingredients: TITANIUM DIOXIDE 8.38%, ETHYLHEXYL METHOXYCINNAMATE 7.00%, ETHYLHEXYL SALICYLATE 3.00%, OCTOCRYLENE 2.00%

INACTIVE INGREDIENT

Inactive ingredients:

ALOE BARBADENSIS LEAF WATER, CYCLOPENTASILOXANE, PHENYL TRIMETHICONE, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, CETYL PEG/PPG-10/1 DIMETHICONE, ACRYLATES/STEARYL ACRYLATE/DIMETHICONE METHACRYLATE COPOLYMER, LAURYL PEG-10 TRIS (TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE, BUTYLENE GLYCOL, 1,2-HEXANEDIOL, NIACINAMIDE, DISTEARDIMONIUM HECTORITE, SODIUM CHLORIDE, 4-METHYLBENZYLIDENE CAMPHOR, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, SYNTHETIC FLUORPHLOGOPITE, STEARIC ACID, PORTULACA OLERACEA EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, DIMETHICONE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, ZINC STEARATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, METHYL METHACRYLATE CROSS POLYMER, SILICA, CI 77492, ALUMINUM HYDROXIDE, TRIETHOXYCAPRYLYLSILANE, CI 77491, ALGAE EXTRACT, ECKLONIA CAVA EXTRACT, ENTEROMORPHA COMPRESSA EXTRACT, CAULERPA LENTILLIFERA EXTRACT, UNDARIA PINNATIFIDA EXTRACT, MENYANTHES TRIFOLIATA LEAF EXTRACT, HYDROLYZED COLLAGEN, WATER, BETA-GLUCAN, BETAINE, ALLANTOIN, MICA, CARMINE, SODIUM HYALURONATE, LACTOBACILLUS/KELP FERMENT FILTRATE, CHLORELLA FERMENT, LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE, TUBER MAGNATUM EXTRACT, CI 77499, ADENOSINE, BACILLUS/CORCHORUS OLITORIOUS LEAF FERMENT FILTRATE, PANAX GINSENG CALLUS CULTURE EXTRACT, DISODIUM EDTA, LECITHIN, GLYCERIN, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, LITSEA CUBEBA FRUIT OIL, SANTALUM ALBUM (SANDALWOOD) OIL, PELARGONIUM GRAVEOLENS FLOWER OIL, ELETTARIA CARDAMOMUM SEED OIL, CEDRUS ATLANTICA BARK OIL, CITRUS AURANTIUM DULCIS (ORANGE) OIL, CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL, ETHYLHEXYLGLYCERIN, CAPRYLYL GLYCOL, PENTYLENE GLYCOL, PHENOXYETHANOL

PURPOSE

Purpose: Sunscreen

WARNINGS

Warnings:

For external use only.

When using cosmetics or after use, consult with a specialist if there is any abnormal symptom or side effect such as red spot, swelling or itching by direct sunlight

Discontinue use if signs of irritation or rashes appear.

Do not use in wounded area.

Keep out of reach of children.

Keep away from direct sunlight.

DESCRIPTION

Uses:

Help brightening

Help anti-wrinkle

Help sunscreen

Directions:

Take an appropriate amount and spread evenly on skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DEOPROCE UV WATERFUL CUSHION NO 13 LIGHT BEIGE 
titanium dioxide, octinoxate, octisalate, octocrylene powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72105-070
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.17 g  in 14 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.98 g  in 14 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.42 g  in 14 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.28 g  in 14 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72105-070-02	2 in 1 CARTON	02/01/2018	11/01/2019
1	NDC: 72105-070-01	14 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	02/01/2018	11/01/2019

Labeler - Greencos Co., Ltd. (694777325)

Registrant - Greencos Co., Ltd. (694777325)

Establishment
Name	Address	ID/FEI	Business Operations
Greencos Co., Ltd.		694777325	manufacture(72105-070)

Revised: 11/2019

Document Id: a80cc810-9c61-4406-ae7f-8c9d8c821e61

34390-5

Set id: 8e914196-ea83-4c02-a19a-441e48eff287

Version: 2

Effective Time: 20191128

 

Greencos Co., Ltd.