UV PROTECTION SUN BLOCK SPF50 PA

Manufacturer
NOKSIBCHO cosmetic Co., Ltd.
Effective date
2020-09-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:16:05

Label at a glance#

ProductUV PROTECTION SUN BLOCK SPF50 PA
Active ingredientTITANIUM DIOXIDE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

titanium dioxide

INACTIVE INGREDIENT SECTION

Water
Aluminum hydroxide
Stearic acid
Cyclomethicone
PEG-10 Dimethicone
Isohexadecane
Micro particle zinc oxide
Methicone
Cyclomethicone
PEG-10 Dimethicone
Ethylhexyl Methoxycinnamate
Dimethicone
Dimethicone/Vinyl Dimethicone Crosspolymer
Isoamyl p-Methoxycinnamate
Cyclopentasiloxane
Malva Sylvestris (Mallow) Flower Extract
4-Methylbenzylidene Camphor
PEG-10 Dimethicone
Sorbitan Sesquioleate
Cetyl PEG/PPG-10/1 Dimethicone
Isononyl Isononanoate
Disteardimonium Hectorite
Beeswax
Ozokerite
Butylene glycol
Sodium Hyaluronate
Leontopodium alpinum extract
Myrciaria Dubia Fruit Extract
Euterpe Oleracea Fruit Extract
Magnesium Sulfate
Aloe Barbadensis Leaf Extract
Camellia Sinensis Leaf Extract
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

1. After smoothing your skin tone with your regular skin care products, apply a small amount of UV Protection Sun Block to your face.
2. Spread it softly on your whole face.
3. It makes your skin tone moist and clean

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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DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73590-005573590-0055-2

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
aecb3934-2ec4-3a96-e053-2a95a90a7767aeb392ea-bb05-7bf7-e053-2a95a90aeaf92020-09-08WarningsExact identifier
spl set id: aeb392ea-bb05-7bf7-e053-2a95a90aeaf9

Reported adverse events (FAERS/openFDA)#

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