Home NDC 58411-894 SHISEIDO REVITALESSENCE SKIN GLOW PRIMER
Product NDC 58411-894
11-digit product format 584110894
Labeler code 58411
Product ID 58411-894_da27f6d7-29e3-461e-ac53-19f12c10c734
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Octinoxate, and Octocrylene
Dosage form EMULSION
Route TOPICAL
Labeler SHISEIDO AMERICAS CORPORATION
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-01-01
Substance AVOBENZONE; OCTINOXATE; OCTOCRYLENE
Active strength .77925; 1.52733; 1.5585 g/30mL; g/30mL; g/30mL
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 REVITALESSENCE SKIN GLOW PRIMER
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE .77925 g/30mL OCTINOXATE 1.52733 g/30mL OCTOCRYLENE 1.5585 g/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup 5A68WGF6WM 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 58411-894-60 SHISEIDO REVITALESSENCE SKIN GLOW PRIMER 30 mL in 1 TUBE EMULSION 30 1 58411-894-60 SHISEIDO REVITALESSENCE SKIN GLOW PRIMER 1 in 1 CARTON EMULSION 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58411-894 SHISEIDO REVITALESSENCE SKIN GLOW PRIMER (AVOBENZONE, OCTINOXATE, AND OCTOCRYLENE) EMULSION [SHISEIDO AMERICAS CORPORATION] 1 Current NDC, 2 package rows 20250316_805fd75e-3c53-4ddd-afdc-a65f921822d4.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 Sample Exclude flag Status 58411-894-60 58411089460 1 TUBE in 1 CARTON (58411-894-60) / 30 mL in 1 TUBE 1 tube 2023-01-01 No No Current