Home NDC 58411-891 SHISEIDO ULTIMATE SUN PROTECTOR
Product NDC 58411-891
11-digit product format 584110891
Labeler code 58411
Product ID 58411-891_47b9d7e2-7a08-f71c-e063-6394a90aef15
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, and OCTOCRYLENE
Dosage form SPRAY
Route TOPICAL
Labeler SHISEIDO AMERICAS CORPORATION
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-03-01
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 3.1533; 13.71; 6.855; 6.855 g/150mL; g/150mL; g/150mL; g/150mL
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 SHISEIDO ULTIMATE SUN PROTECTOR
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3.1533 g/150mL HOMOSALATE 13.71 g/150mL OCTISALATE 6.855 g/150mL OCTOCRYLENE 6.855 g/150mL
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58411-891-20 SHISEIDO ULTIMATE SUN PROTECTOR 150 mL in 1 CARTRIDGE SPRAY 150 2
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 58411-891-20 58411089120 150 mL in 1 CARTRIDGE (58411-891-20) 150 ml 2024-03-01 No No Current