Home NDC 70319-240 COSRX
Product NDC 70319-240
11-digit product format 703190240
Labeler code 70319
Product ID 70319-240_4840f608-944b-3e3d-e063-6394a90a1d9d
Type HUMAN OTC DRUG
Nonproprietary name Vitamin E Vitalizing Sunscreen
Dosage form LOTION
Route TOPICAL
Labeler COSRX inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-19
Substance OCTISALATE; AVOBENZONE; OCTOCRYLENE; HOMOSALATE
Active strength 2.25; 1.25; 4.5; 4.5 mg/50mL; mg/50mL; mg/50mL; mg/50mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base COSRX
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 2.25 mg/50mL AVOBENZONE 1.25 mg/50mL OCTOCRYLENE 4.5 mg/50mL HOMOSALATE 4.5 mg/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70319-240-01 COSRX 50 mL in 1 TUBE LOTION 50 1 70319-240-01 COSRX 1 in 1 CARTON LOTION 1 1
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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70319-240-01 70319024001 1 TUBE in 1 CARTON (70319-240-01) / 50 mL in 1 TUBE 1 tube 2026-01-19 No No Current