Home NDC 58411-657 SHISEIDO FUTURE Solution LX INFINITE TREATMENT PRIMER
Product NDC 58411-657
11-digit product format 584110657
Labeler code 58411
Product ID 58411-657_47b9be75-c9c2-b19a-e063-6294a90a3412
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE, OCTINOXATE, and ENSULIZOLE
Dosage form EMULSION
Route TOPICAL
Labeler SHISEIDO AMERICAS CORPORATION
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-05-01
Substance TITANIUM DIOXIDE; OCTINOXATE; ENSULIZOLE
Active strength 1.77; 1.71; .428 g/40mL; g/40mL; g/40mL
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 FUTURE Solution LX INFINITE TREATMENT PRIMER
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 1.77 g/40mL OCTINOXATE 1.71 g/40mL ENSULIZOLE .428 g/40mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup 9YQ9DI1W42 Internal UNII lookup
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 58411-657-10 SHISEIDO FUTURE Solution LX INFINITE TREATMENT PRIMER 40 mL in 1 TUBE EMULSION 40 3 58411-657-10 SHISEIDO FUTURE Solution LX INFINITE TREATMENT PRIMER 1 in 1 CARTON EMULSION 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58411-657 SHISEIDO FUTURE SOLUTION LX INFINITE TREATMENT PRIMER (TITANIUM DIOXIDE, OCTINOXATE, AND ENSULIZOLE) EMULSION [SHISEIDO AMERICAS CORPORATION] 2 Current NDC, Legacy NDC, 2 package rows 20241228_ff088b0c-27c9-4ea8-bf94-6261378c7190.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 58411-657-10 58411065710 1 TUBE in 1 CARTON (58411-657-10) / 40 mL in 1 TUBE 1 tube 2021-05-01 0000-00-00 No No Current