Shiseido White Lucent Day Emulsion
Product Images NDC 58411-463

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Shiseido White Lucent Day (NDC 58411-463). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Shiseido Americas Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Principal Display Panel (50 mL Tube Carton)

Packaging label for SHISEIDO WHITE LUCENT DAY EMULSION Broad Spectrum SPF 23 sunscreen, topical emulsion in a 50 mL (1.7 oz) size. The label highlights the product's ReNeura Technology+, usage directions, active ingredients (Avobenzone 2.5%, Octinoxate 7.4%, Octocrylene 3.0%), warnings, inactive ingredients, and manufacturer, Shiseido Americas Corporation, with address in New York, NY. The label includes Drug Facts, usage instructions, and contact information.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.