Home NDC 58411-481 SHISEIDO ULTIMATE SUN PROTECTOR
Product NDC 58411-481
11-digit product format 584110481
Labeler code 58411
Product ID 58411-481_e6522904-8d36-4733-bc3e-7eae181fc7a8
Type HUMAN OTC DRUG
Nonproprietary name octisalate, homosalate, octocrylene, and avobenzone
Dosage form LOTION
Route TOPICAL
Labeler SHISEIDO AMERICAS CORPORATION
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance OCTISALATE; HOMOSALATE; OCTOCRYLENE; AVOBENZONE
Active strength 50; 100; 50; 23 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 50 mg/mL HOMOSALATE 100 mg/mL OCTOCRYLENE 50 mg/mL AVOBENZONE 23 mg/mL
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 58411-481-10 SHISEIDO ULTIMATE SUN PROTECTOR 1 in 1 CARTON LOTION 1 5 58411-481-10 SHISEIDO ULTIMATE SUN PROTECTOR 150 mL in 1 BOTTLE LOTION 150 5 58411-481-11 SHISEIDO ULTIMATE SUN PROTECTOR 50 mL in 1 BOTTLE LOTION 50 5 58411-481-11 SHISEIDO ULTIMATE SUN PROTECTOR 1 in 1 CARTON LOTION 1 5 58411-481-12 SHISEIDO ULTIMATE SUN PROTECTOR 1 in 1 CARTON LOTION 1 5 58411-481-12 SHISEIDO ULTIMATE SUN PROTECTOR 300 mL in 1 BOTTLE LOTION 300 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58411-481 SHISEIDO ULTIMATE SUN PROTECTOR (OCTISALATE, HOMOSALATE, OCTOCRYLENE, AND AVOBENZONE) LOTION [SHISEIDO AMERICAS CORPORATION] 5 Current NDC, Legacy NDC, 6 package rows 20250322_7a98171f-bf21-40d4-bc78-883aa0b0c438.zip
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 Marketing end Sample Exclude flag Status 58411-481-10 58411048110 1 BOTTLE in 1 CARTON (58411-481-10) / 150 mL in 1 BOTTLE 1 bottle 2020-01-01 0000-00-00 No No Current 58411-481-11 58411048111 1 BOTTLE in 1 CARTON (58411-481-11) / 50 mL in 1 BOTTLE 1 bottle 2020-01-01 0000-00-00 No No Current 58411-481-12 58411048112 1 BOTTLE in 1 CARTON (58411-481-12) / 300 mL in 1 BOTTLE 1 bottle 2020-01-01 No No Current