DEOPROCE UV WATERFUL CUSHION NO 21 Natural Beige by Greencos Co., Ltd.

DEOPROCE UV WATERFUL CUSHION NO 21 Natural Beige by

Drug Labeling and Warnings

DEOPROCE UV WATERFUL CUSHION NO 21 Natural 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 21 NATURAL 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, CI 77492, ALOE BARBADENSIS LEAF EXTRACT, DIMETHICONE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER ZINC STEARATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, METHYL METHACRYLATE CROSS POLYMER, SILICA, CI 77491, ALUMINUM HYDROXIDE, TRIETHOXYCAPRYLYLSILANE, 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, ADENOSINE, BACILLUS/CORCHORUS OLITORIOUS LEAF FERMENT FILTRATE, PANAX GINSENG CALLUS CULTURE EXTRACT, DISODIUM EDTA, LECITHIN, GLYCERIN, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, CI 77499, 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

Image of carton

DEOPROCE UV WATERFUL CUSHION NO 21 NATURAL BEIGE 
titanium dioxide, octinoxate, octisalate, octocrylene powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72105-080
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE1.17 g  in 14 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE0.98 g  in 14 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE0.42 g  in 14 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE0.28 g  in 14 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72105-080-022 in 1 CARTON02/01/201811/01/2019
1NDC: 72105-080-0114 g in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35202/01/201811/01/2019
Labeler - Greencos Co., Ltd. (694777325)
Registrant - Greencos Co., Ltd. (694777325)
Establishment
NameAddressID/FEIBusiness Operations
Greencos Co., Ltd.694777325manufacture(72105-080)

Revised: 11/2019
 
Greencos Co., Ltd.