Shiseido Future Lx Total Radiance Foundation E Cream
Product Images NDC 58411-336

11 FDA label images from Shiseido Americas Corporation · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Shiseido Future Lx Total Radiance Foundation E (NDC 58411-336). 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 (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
Packaging label for SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E Golden 1 cream with active ingredient octinoxate 5.9%. This 30mL topical sunscreen has Broad Spectrum SPF 20 and is labeled by Shiseido Americas Corporation. The label includes usage directions, drug facts, warnings, and inactive ingredient information in English.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E Golden 2 cream with Octinoxate 5.9% as the active ingredient. This topical sunscreen product offers Broad Spectrum SPF 20 protection and is presented in a 30 mL (1.2 oz) container. The label shows the brand Shiseido Ginza Tokyo and includes detailed drug facts, directions, warnings, and inactive ingredients, with the manufacturer listed as Shiseido Americas Corporation.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
Packaging label for SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E Golden 2 cream, containing octinoxate 5.9% as the active ingredient. It is a broad spectrum SPF 20 sunscreen, presented in a 30mL (1.2 oz.) container. The product is labeled as topical, produced by Shiseido Americas Corporation, with directions, uses, warnings, inactive ingredients, and contact information included on the label.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
Packaging label for SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E Golden 4 cream, a topical sunscreen product with Octinoxate 5.9% as the active ingredient. The 30mL (1.2 oz) container provides Broad Spectrum SPF 20 protection. Labeler is Shiseido Americas Corporation. The label includes drug facts, directions, warnings, ingredients, and contact information.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E Golden 2 cream sunscreen packaged in a 30 mL (1.2 oz) container. The product lists octinoxate 5.9% as the active sunscreen ingredient and provides broad spectrum SPF 20 protection. The label includes directions for use, warnings, inactive ingredients, and contact information. Manufactured by SHISEIDO AMERICAS CORPORATION, New York, USA, with formulation by Shiseido Laboratories, Japan.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
Packaging label for SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E Golden 2 cream, a topical human OTC drug containing Octinoxate 5.9% as active ingredient. The product provides Broad Spectrum SPF 20 sunscreen protection and is supplied in a 30 mL (1.2 oz.) container. The label includes drug facts, directions, inactive ingredients, uses, warnings, and manufacturer information for Shiseido Americas Corporation.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
Packaging label for SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E Golden 2, a topical cream sunscreen containing Octinoxate 5.9% as the active ingredient. The product is labeled as Broad Spectrum SPF 20 sunscreen with a net volume of 30 mL (1.2 oz). The labeler is SHISEIDO AMERICAS CORPORATION. The label includes usage directions, warnings, inactive ingredients, and contact information.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
Packaging label for SHISEIDO FUTURE SOLUTION LX Total Radiance Foundation E Golden 2, a cream topical sunscreen with broad spectrum SPF 20. The label highlights the active ingredient Octinoxate 5.9%, net weight 30 mL (1.2 oz). Manufactured by Shiseido Americas Corporation, it includes Drug Facts, directions, warnings, and other product information.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
SHISEIDO FUTURE SOLUTION LX Total Radiance Foundation E Golden 2, a cream topical sunscreen with active ingredient Octinoxate 5.9%, Broad Spectrum SPF 20. The 30 mL (1.2 oz) container is labeled as produced by Shiseido Americas Corporation. The packaging includes directions for use, drug facts, and inactive ingredients, emphasizing skin protection and sun safety.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
SHISEIDO FUTURE SOLUTION LX Total Radiance Foundation E Golden 2 cream SPF 20 sunscreen, 30mL (1.2 OZ) carton label. The packaging describes the product as a broad spectrum sunscreen with active ingredient Octinoxate 5.9%. Labeler is SHISEIDO AMERICAS CORPORATION. The label includes directions for use, active and inactive ingredients, uses, warnings, and contact information.*
FDA Label Image

Principal Display Panel (30 mL Jar Carton)

Principal Display Panel (30 mL Jar Carton)
Packaging label for SHISEIDO FUTURE SOLUTION LX Total Radiance Foundation E Golden 2, a broad spectrum SPF 20 sunscreen cream with active ingredient Octinoxate 5.9%. The label includes product name, strength (approx 1832 mg/30mL based on product data), directions for sunscreen use, inactive ingredients, warnings, and manufacturer Shiseido Americas Corporation. The package size is 30mL (1.2 OZ).*

* 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.