Home NDC 58411-952 SHISEIDO URBAN ENVIRONMENT
Product NDC 58411-952
11-digit product format 584110952
Labeler code 58411
Product ID 58411-952_4617da57-c5ae-99fc-e063-6394a90ac726
Type HUMAN OTC DRUG
Nonproprietary name Ensulizole, Homosalate, Octisalate, Zinc OXide
Dosage form EMULSION
Route TOPICAL
Labeler Shiseido Americas Corporation
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-11
Substance ENSULIZOLE; HOMOSALATE; OCTISALATE; ZINC OXIDE
Active strength .6; 9; 3; 9.3 g/50mL; g/50mL; g/50mL; g/50mL
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 URBAN ENVIRONMENT
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ENSULIZOLE .6 g/50mL HOMOSALATE 9 g/50mL OCTISALATE 3 g/50mL ZINC OXIDE 9.3 g/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 58411-952-10 SHISEIDO URBAN ENVIRONMENT 50 mL in 1 BOTTLE, PLASTIC EMULSION 50 2 58411-952-10 SHISEIDO URBAN ENVIRONMENT 1 in 1 BOX EMULSION 1 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 Status 58411-952-10 58411095210 50 mL in 1 BOTTLE, PLASTIC 50 ml Historical