FDA.reportPublic FDA data

DEOPROCE HYALURONIC COOLING SUN

Manufacturer
Greencos Co., Ltd.
Effective date
2019-12-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:47:48

Label at a glance#

ProductDEOPROCE HYALURONIC COOLING SUN
Active ingredientOCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

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

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

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

DESCRIPTION SECTION

Uses:

Help sunscreen

Directions:

Take an appropriate amount and spread evenly on skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72105-06072105-060-01, 72105-060-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
DIPROPYLENE GLYCOLE107L85C40IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d7a60a71-a693-4fb0-9502-6c38b581cc30d98cf52a-3584-46be-a7bf-0eae39bd99c92021-05-25WarningsExact identifier
spl set id: d98cf52a-3584-46be-a7bf-0eae39bd99c9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.