COSRX

Manufacturer
COSRX inc.
Effective date
2025-05-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:01:17

Label at a glance#

ProductCOSRX
Active ingredientOCTISALATE, OCTOCRYLENE, AVOBENZONE, HOMOSALATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.80%

Homosalate 11.00%

Octisalate 4.50%

Octocrylene 7.50%

OTC - PURPOSE SECTION

SUNSCREEN STICK

OTC - WHEN USING SECTION

helps prevent sunburn.

WARNINGS SECTION

For external use only.
Do not use on damaged or broken skin.
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DESCRIPTION SECTION

apply liberally 15 minutes before sun exposure
reapply :
after 80 minutes of swimming or sweating

immediately after towel drying

at least every 2 hours

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging.
To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
limit time in the sun, especially from 10 a.m. – 2 p.m.
wear long- sleeved shirts, pants, hats, and sunglasses

children under 6 months of age : Ask a doctor

INDICATIONS & USAGE SECTION

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun.

INACTIVE INGREDIENT SECTION

Diethylhexyl Carbonate, Methyl Methacrylate Crosspolymer, Synthetic Wax, Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Butyloctyl Salicylate, Isopropyl Palmitate, Diisostearyl Malate, Dimethiconol, Trisiloxane, Diphenylsiloxy Phenyl Trimethicone, Ethylhexyl Isononanoate, Synthetic Fluorphlogopite, Polyethylene, Polymethylsilsesquioxane, Bis-Behenyl/Isostearyl /Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Ethylene/Propylene Copolymer, Camellia Japonica Seed Oil, Silica Dimethyl Silylate, Dimethicone Crosspolymer, Candelilla Wax Esters, Copernicia Cerifera (Carnauba) Wax, 3-O-Ethyl Ascorbic Acid, Panthenol, Sodium Hyaluronate, Tocopheryl Acetate

OTC - QUESTIONS SECTION

global@cosrx.co.kr

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AIRY-LIGHT CLEAR
SUNSCREEN STICK

Vitamin E&C + Panthenol
+ Hyaluronic Acid

Amazing Lightness!
+ Photo-aging & Free Radical Care
+ No White Cast

SPF50 BROAD SPECTRUM

WATER RESISTANT (80 MINUTES)

COSRX

19 g / 0.67 oz. AIRY LIGHT CLEAR SUNSCREEN STICKAIRY LIGHT CLEAR SUNSCREEN STICK

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70319-230-01COSRX1 in 1 CARTONSTICK13
70319-230-01COSRX19 g in 1 BOTTLE, PLASTICSTICK193

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70319-230COSRX (AIRY-LIGHT CLEAR SUNCREEN STICK) STICK [COSRX INC.]3Current NDC, 2 package rows20250522_313b1a73-8863-c458-e063-6394a90a01d6.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70319-23070319-230-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
COSRXAIRY-LIGHT CLEAR SUNCREEN STICKCOSRX inc.313b1a73-8863-c458-e063-6394a90a01d62025-05-20WarningsExact identifier
ndc (package): 70319-230-01
ndc (product): 70319-230
ndc11 (package): 70319023001
spl id: 358a61fb-86b7-934e-e063-6394a90afe07
spl set id: 313b1a73-8863-c458-e063-6394a90a01d6

Reported adverse events (FAERS/openFDA)#

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