Home NDC 87582-004 ORLASKIN HYDRATING SUNSCREEN SPF 50
Product NDC 87582-004
11-digit product format 875820004
Labeler code 87582
Product ID 87582-004_552b4c87-4622-d5a7-e063-6294a90a042e
Type HUMAN OTC DRUG
Nonproprietary name Octocrylene Ethylhexyl Methoxycinnamate Ethylhexyl Salicylate Avobenzone
Dosage form SPRAY
Route TOPICAL
Labeler Guangzhou Yapheon Health Industry Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-27
Substance OCTOCRYLENE; ETHYLHEXYL METHOXYCINNAMATE; ETHYLHEXYL SALICYLATE; AVOBENZONE
Active strength 10; 7; 5; 3 g/100mL; g/100mL; g/100mL; g/100mL
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 ORLASKIN HYDRATING SUNSCREEN SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 10 g/100mL ETHYLHEXYL METHOXYCINNAMATE 7 g/100mL ETHYLHEXYL SALICYLATE 5 g/100mL AVOBENZONE 3 g/100mL
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.
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 87582-004-01 87582000401 100 mL in 1 BOTTLE, SPRAY (87582-004-01) 100 ml 2026-06-27 No No Current