LUACELL Illuminating White Label Sun Cream

Manufacturer: EYESOME. Co.,Ltd.
Effective date: 2019-08-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:13:06

Label at a glance#

ProductLUACELL Illuminating White Label Sun Cream

Active ingredientOCTOCRYLENE, OCTISALATE, AVOBENZONE, HOMOSALATE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Homosalate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Octocrylene

INACTIVE INGREDIENT SECTION

Water, Dimethicone, Slica, etc

OTC - PURPOSE SECTION

Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Take an appropriate amount, spread it gently according to the skin texture, and tap it softly to absorb it.

WARNINGS SECTION

Do not use on broken or irritated skin
Storage & Handling
1) Keep out of reach from children
2) Keep out of sunlight
3) Avoid contact with eyes

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

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

LUACELL Illuminating White Label Sun Cream
Homosalate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Octocrylene
WATER
DIMETHICONE
OCTOCRYLENE
OCTISALATE
AVOBENZONE
HOMOSALATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58832-0001	58832-0001-1

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
DIMETHICONE	92RU3N3Y1O	IACT
OCTOCRYLENE	5A68WGF6WM	ACTIB
OCTISALATE	4X49Y0596W	ACTIB
AVOBENZONE	G63QQF2NOX	ACTIB
HOMOSALATE	V06SV4M95S	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b7953fc8-3f32-464c-e053-2a95a90a23c9			91392b71-79bb-2302-e053-2a95a90a89be	2020-12-29	Warnings	Exact identifier spl set id: 91392b71-79bb-2302-e053-2a95a90a89be

Reported adverse events (FAERS/openFDA)#

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