DEOPROCE HYALURONIC COOLING SUN- octinoxate, octocrylene, octisalate, avobenzone gel

DEOPROCE HYALURONIC COOLING SUN by

Drug Labeling and Warnings

DEOPROCE HYALURONIC COOLING SUN by is a Otc medication manufactured, distributed, or labeled by Greencos Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: ETHYLHEXYL METHOXYCINNAMATE 7.00%, OCTOCRYLENE 4.00%, ETHYLHEXYL SALICYLATE 4.00%, BUTYL METHOXYDIBENZOYLMETHANE 3.00%

INACTIVE INGREDIENT

Inactive ingredients:

WATER, 4-METHYLBENZYLIDENE CAMPHOR, BEHENYL ALCOHOL, DIPROPYLENE GLYCOL, 1,2-HEXANEDIOL, NIACINAMIDE, GLYCERIN, METHYL METHACRYLATE CROSSPOLYMER, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, PORTULACA OLERACEA EXTRACT, OLEA EUROPAEA (OLIVE) LEAF EXTRACT, SODIUM HYALURONATE, CERAMIDE NP, SEA WATER, BAMBUSA VULGARIS EXTRACT, EUCALYPTUS GLOBULUS LEAF EXTRACT, HYDROGENATED LECITHIN, ALOE BARBADENSIS LEAF EXTRACT, ADANSONIA DIGITATA SEED EXTRACT, BUTYLENE GLYCOL, TROMETHAMINE, CARBOMER, FRAGRANCE, SILICA, ADENOSINE, DISODIUM EDTA, PENTYLENE GLYCOL, PHENOXYETHANOL, CAPRYLYL GLYCOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, ETHYLHEXYLGLYCERIN, LIMONENE, LINALOOL

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 sunscreen

Directions:

Take an appropriate amount and spread evenly on skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEOPROCE HYALURONIC COOLING SUN 
octinoxate, octocrylene, octisalate, avobenzone gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72105-060
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	3.50 g  in 50 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.00 g  in 50 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.00 g  in 50 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.50 g  in 50 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72105-060-02	1 in 1 CARTON	02/01/2018
1	NDC: 72105-060-01	50 g in 1 TUBE; 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

Labeler - Greencos Co., Ltd. (694777325)

Registrant - Greencos Co., Ltd. (694777325)

Establishment
Name	Address	ID/FEI	Business Operations
Greencos Co., Ltd.		694777325	manufacture(72105-060)