EX CUSEME Brightening SunCream

Manufacturer: BBC Inc
Effective date: 2020-10-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:31:53

Label at a glance#

ProductEX CUSEME Brightening SunCream

Active ingredientTITANIUM DIOXIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

titanium dioxide

OTC - PURPOSE SECTION

UV protection

skin whitening

wrinkle care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

WARNINGS SECTION

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

Sambucus Nigra Flower Extract
Glycerin
1,2-Hexanediol
Ethylhexylglycerin
Glycerin
Ethylhexyl Methoxycinnamate
Ethylhexyl Salicylate
Cyclopentasiloxane
Cyclohexasiloxane
Centella Asiatica Extract
1,2-Hexanediol
Dicaprylyl Carbonate
Aluminum Hydroxide
Stearic Acid
Niacinamide
Butylene Glycol
Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine
Diethylamino Hydroxybenzoyl Hexyl Benzoate
Cetearyl Alcohol
1,2-Hexanediol
Arachidyl Alcohol
Behenyl Alcohol
Arachidyl Glucoside
Phenyl Trimethicone
Caulerpa Lentillifera Extract
Sea Cucumber Extract
1,2-Hexanediol
Paeonia Suffruticosa Root Extract
Schisandra Chinensis Fruit Extract
Lycium Chinense Fruit Extract
1,2-Hexanediol
Sambucus Nigra Flower Extract
Chamomilla Recutita (Matricaria) Flower Extract
Calendula Officinalis Flower Extract
1,2-Hexanediol
Glyceryl Stearate
Stearic Acid
Potassium Cetyl Phosphate
Polymethyl Methacrylate
Ammonium Acryloyldimethyltaurate/VP Copolymer
Xanthan Gum
Dipropylene glycol
Lavandula hybrida oil
Pelargonium graveolens flower oil
Rosmarinus officinalis (rosemary) leaf oil
Eucalyptus globulus leaf oil
Tromethamine
Carbomer
Adenosine
Dipotassium Glycyrrhizate
Disodium EDTA
Panthenol
rh-Oligopeptide-1
Ceramide NP
(-)-Alpha-Bisabolol

INDICATIONS & USAGE SECTION

apply proper amount to the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
80785-0001-1	2023-01-30	C162847	48780-1	f386c649-dd4e-0266-e053-dadaa90a7c1a	b1e63aa4-2226-b0e9-e053-2995a90a3c8b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80785-0001-1	EX CUSEME Brightening SunCream	75 g in 1 TUBE	CREAM	75		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80785-0001	EX CUSEME BRIGHTENING SUNCREAM (TITANIUM DIOXIDE) CREAM [BBC INC]	1	Legacy NDC, 1 package rows	20201018_b1e63aa4-2226-b0e9-e053-2995a90a3c8b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

EX CUSEME Brightening SunCream
titanium dioxide
ALUMINUM HYDROXIDE
WATER
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80785-0001	80785-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TITANIUM DIOXIDE	15FIX9V2JP	ACTIB
ALUMINUM HYDROXIDE	5QB0T2IUN0	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT

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
b1e63a2f-a0da-78fd-e053-2a95a90a0695			b1e63aa4-2226-b0e9-e053-2995a90a3c8b	2020-10-17	Warnings	Exact identifier spl id: b1e63a2f-a0da-78fd-e053-2a95a90a0695 spl set id: b1e63aa4-2226-b0e9-e053-2995a90a3c8b

Reported adverse events (FAERS/openFDA)#

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