COXIR CERAMIDE DAILY UV SUN BLOCK

Manufacturer
NOKSIBCHO cosmetic Co., Ltd.
Effective date
2020-09-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:05

Label at a glance#

ProductCOXIR CERAMIDE DAILY UV SUN BLOCK
Active ingredientTITANIUM DIOXIDE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

titanium dioxide

INACTIVE INGREDIENT SECTION

Micro particle titanium dioxide
Aluminum hydroxide
Stearic acid
Cyclomethicone
PEG-10 Dimethicone
Isohexadecane
Micro particle zinc oxide
Methicone
Cyclomethicone
PEG-10 Dimethicone
Ethylhexyl Methoxycinnamate
Isoamyl p-Methoxycinnamate
Cyclopentasiloxane
4-Methylbenzylidene Camphor
PEG-10 Dimethicone
Glycerin
Cetyl PEG/PPG-10/1 Dimethicone
Disteardimonium Hectorite
Isononyl Isononanoate
Beeswax
Ozokerite
Sodium Hyaluronate
Aloe Barbadensis Leaf Extract
Camellia Sinensis Leaf Extract
Collagen Extract
Myrciaria Dubia Fruit Extract
Euterpe Oleracea Fruit Extract
Magnesium Sulfate
Hydrogenated Lecithin
Linoleic acid
Water
Glycerin
Ceramide NP
TEA-cocoyl Glutamate
Caprylic/capric Triglyceride
Camellia Japonica seed oil
Phenoxyethanol
Ethylhexylglycerin
Parfum

OTC - PURPOSE SECTION

sun block

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Can be used daily 15 minutes before sun exposure. Apply evenly to face and neck. Always reapply as needed.

WARNINGS SECTION

For external use only
When using this product

■ if the following symptoms occurs after use, stop use and consult with a skin specialist

red specks, swelling, itching

■ don’t use on the part where there is injury, eczema, or dermatitis

Keep out of reach of children

■ if swallowed, get medical help or contact a person control center immediately

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73590-005673590-0056-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

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
aecb52c5-b306-9234-e053-2995a90a5835aeb392ea-bb0f-7bf7-e053-2a95a90aeaf92020-09-08WarningsExact identifier
spl set id: aeb392ea-bb0f-7bf7-e053-2a95a90aeaf9

Reported adverse events (FAERS/openFDA)#

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