Home NDC 58411-924 SHISEIDO ULTIMATE SUN PROTECTION S
Product NDC 58411-924
11-digit product format 584110924
Labeler code 58411
Product ID 58411-924_372678b6-f2b4-f456-e063-6294a90a2cbe
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide and Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Shiseido Americas Corporation
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-09
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 11.6116; 24.6268 g/100mL; g/100mL
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 PROTECTION S
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 11.6116 g/100mL ZINC OXIDE 24.6268 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z Internal UNII lookup
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 58411-924-10 SHISEIDO ULTIMATE SUN PROTECTION S 1 in 1 CARTON LOTION 1 2 58411-924-10 SHISEIDO ULTIMATE SUN PROTECTION S 100 mL in 1 BOTTLE LOTION 100 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 Status 58411-924-10 58411092410 1 in 1 CARTON Historical