Shiseido Revitalessence Skin Glow Foundation Emulsion
Product Images NDC 58411-863

Product Visual Gallery

This gallery contains 29 technical images submitted to the FDA as part of the official labeling for Shiseido Revitalessence Skin Glow Foundation (NDC 58411-863). 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 Container Carton)

SHISEIDO REVITALESSENCE SKIN GLOW Foundation 2.30805 g/30mL emulsion sunscreen with broad spectrum SPF30. The packaging label features product branding, ingredient highlights including Fermented Kefir and Niacinamide, active ingredient Octinoxate 6.9%, use and warning instructions, and manufacturer information by Shiseido Americas Corporation. The label indicates the product is fragrance free, suitable for sensitive skin, and dermatologist tested.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

The packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 120 features a 30mL emulsion sunscreen with octinoxate as the active ingredient (6.9%). It includes broad spectrum SPF 30 protection, Bio-BoostRED Technology, fermented kefir, and niacinamide. The label displays the product name, directions, warnings, inactive ingredients, and manufacturer SHISEIDO AMERICAS CORPORATION. The design includes both English and Japanese text and emphasizes suitability for all skin types, including sensitive skin.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

The image shows the packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 120, a 30 mL topical emulsion containing 2.30805 g/30 mL of Octinoxate. The label indicates it is a broad spectrum SPF 30 sunscreen with Bio-BoostRED Technology, Fermented Kefir+, and Niacinamide. The manufacturer is Shiseido Americas Corporation.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

SHISEIDO REVITALESSENCE SKIN GLOW Foundation 30mL emulsion containing 2.30805 g/30mL Octinoxate as the active ingredient. The label indicates it is a broad spectrum SPF30 sunscreen with Bio-BoostRED Technology, fermented kefir, and niacinamide. The labeler is SHISEIDO AMERICAS CORPORATION. Directions, drug facts, warnings, and inactive ingredients are printed on the packaging.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation emulsion, a topical sunscreen containing 2.30805 g/30mL of Octinoxate, labeled with SPF 30 and broad spectrum protection. The 30 mL bottle includes Bio-BoostRED Technology with Fermented Kefir and Niacinamide. Manufactured by Shiseido Americas Corporation.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

SHISEIDO REVITALESSENCE SKIN GLOW Foundation 2.30805 g/30mL emulsion sunscreen with broad spectrum SPF30. The packaging highlights Bio-BoostRED Technology with Fermented Kefir+ Niacinamide, offering medium coverage and a 12-hour wear. Label includes drug facts, active ingredient Octinoxate 6.9%, usage directions, warnings, and manufacturer SHISEIDO AMERICAS CORPORATION. The product is fragrance free and suitable for all skin types.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation emulsion SPF 30 with 2.30805 g/30mL octinoxate. The label states broad spectrum sunscreen with Bio-BoostRED Technology, Fermented Kefir, and Niacinamide. Manufactured by SHISEIDO AMERICAS CORPORATION, the product volume is 30 mL (1 FL. OZ.). The label includes Drug Facts, directions for use, warnings, and inactive ingredients.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 2.30805 g/30mL topical emulsion sunscreen. The box displays the product name, broad spectrum SPF30, Bio-BoostRED Technology, and ingredients Fermented Kefir+ Niacinamide. Labeler information is SHISEIDO AMERICAS CORPORATION. The carton includes Drug Facts, directions for use, warnings, and other informational text.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation, a 30mL topical emulsion containing OCTINOXATE 6.9% as the active sunscreen ingredient. The label highlights broad spectrum SPF 30, Bio-BoostRED Technology, Fermented Kefir+ Niacinamide, and medium coverage with 12-hour wear. Manufactured by Shiseido Americas Corporation.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation, a 30 mL topical emulsion containing octinoxate as the active sunscreen ingredient (6.9%). The label highlights broad spectrum SPF 30 protection, Bio-BoostRED Technology, and key skincare ingredients including Fermented Kefir and Niacinamide. Manufactured by Shiseido Americas Corporation.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 2.30805 g/30mL emulsion sunscreen. The label highlights broad spectrum SPF 30 protection, Bio-BoostRED Technology, and ingredients Fermented Kefir and Niacinamide. Directions and drug facts including active ingredient Octinoxate 6.9% are also included. Labeler is SHISEIDO AMERICAS CORPORATION.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 120, a topical emulsion sunscreen with octinoxate 6.9% as the active ingredient. The product offers broad spectrum SPF30 protection and contains bio-boost red technology, fermented kefir, and niacinamide. The label includes directions for use, warnings, inactive ingredients, and manufacturer information from SHISEIDO AMERICAS CORPORATION. The package size is 30 mL (1 FL OZ).*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 120, an emulsion topical sunscreen containing octinoxate 2.30805 g/30 mL. The label highlights broad spectrum SPF30 protection, Bio-BoostRED Technology, Fermented Kefir+, and Niacinamide. It also includes manufacturer information for Shiseido Americas Corporation, directions, warnings, Drug Facts, and recycling information.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 2.30805 g/30mL emulsion. The label indicates it is a broad spectrum SPF30 sunscreen with Bio-BoostRED Technology and contains Fermented Kefir and Niacinamide. The labeler is SHISEIDO AMERICAS CORPORATION, and the product is intended for topical use. The label includes detailed drug facts, directions, warnings, and inactive ingredients.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 2.30805 g/30mL topical emulsion with Octinoxate as the active ingredient. The label indicates broad spectrum SPF 30 sunscreen protection, highlighting Bio-BoostRED Technology with Fermented Kefir and Niacinamide, suitable for all skin types. Distributed by Shiseido Americas Corporation, the label includes directions, warnings, inactive ingredients, and recycling information.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation emulsion, containing 30 mL (1 FL. OZ.). The label highlights sunscreen broad spectrum SPF30 with active ingredient Octinoxate 6.9%, powered by Fermented Kefir and Niacinamide. It is marketed by SHISEIDO AMERICAS CORPORATION. The label includes directions, drug facts, inactive ingredients, and consumer information, emphasizing suitability for all skin types including sensitive skin.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation emulsion, containing 30 mL (1 FL. OZ.) with broad spectrum SPF30 sunscreen. The label highlights Bio-BoostRED Technology with fermented kefir and niacinamide, suitable for daily sun protection. Labeler is SHISEIDO AMERICAS CORPORATION. Product includes directions, drug facts, and inactive ingredient details.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

The packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation, an emulsion topical sunscreen with 2.30805 g/30mL strength. The label highlights broad spectrum SPF 30, Bio-BoostRED Technology, Fermented Kefir, and Niacinamide. It lists Octinoxate 6.9% as the active ingredient and includes product warnings, directions, inactive ingredients, and manufacturer details for SHISEIDO AMERICAS CORPORATION.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

The image shows the packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation, an emulsion sunscreen with broad spectrum SPF30. The 30 mL (1 FL. OZ.) product contains 2.30805 g/30mL octinoxate as the active ingredient. It is labeled by SHISEIDO AMERICAS CORPORATION and highlights Bio-BoostRED Technology, fermented kefir, and niacinamide. The label includes drug facts, directions, warnings, and contact information.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

The packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 120 shows a 30mL (1 FL. OZ.) emulsion sunscreen containing the active ingredient Octinoxate 6.9%. It features broad spectrum SPF 30 protection and highlights Bio-BoostRED Technology with Fermented Kefir and Niacinamide. Labeler information is SHISEIDO AMERICAS CORPORATION and the product is made in the U.S.A.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 2.30805 g/30mL emulsion with broad spectrum SPF 30 sunscreen. The box highlights the use of Bio-BoostRED Technology with Fermented Kefir+ and Niacinamide. Manufacturer is SHISEIDO AMERICAS CORPORATION. Additional features include directions for use, Drug Facts with active ingredient Octinoxate, warnings, and recycling information.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 2.30805 g/30mL emulsion. The label highlights the product as a broad spectrum SPF30 sunscreen with Bio-BoostRED Technology, Fermented Kefir, and Niacinamide. It includes Shiseido Americas Corporation as the labeler and provides drug facts, directions, warnings, and inactive ingredient information. The 30 mL (1 FL. OZ.) container features Japanese text and branding elements.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation, an emulsion topical sunscreen containing octinoxate at 2.30805 g/30mL. The product has broad spectrum SPF 30 and is labeled as a skincare-active foundation with Bio-BoostRED Technology, fermented kefir, and niacinamide. The labeler is SHISEIDO AMERICAS CORPORATION.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation, an emulsion sunscreen with Octinoxate 6.9% topical. The label indicates broad spectrum SPF30 protection, 30 mL (1 FL OZ) volume, and highlights Bio-BoostRED Technology with Fermented Kefir and Niacinamide. Labeler is SHISEIDO AMERICAS CORPORATION, New York, NY, USA.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation emulsion, containing octinoxate 2.30805 g/30mL as the active ingredient. The product is a topical sunscreen with broad spectrum SPF 30, featuring Bio-BoostRED Technology, Fermented Kefir+, and Niacinamide. It is labeled with directions, drug facts, and warnings, manufactured by Shiseido Americas Corporation. The container size is 30mL (1 FL. OZ.).*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation, an emulsion topical sunscreen with OCTINOXATE 6.9% as the active ingredient. The product contains 30 mL (1 FL. OZ.) and provides broad spectrum SPF30 protection. The label highlights Bio-BoostRED Technology, Fermented Kefir, and Niacinamide. It is distributed by SHISEIDO AMERICAS CORPORATION.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation, an emulsion topical sunscreen with broad spectrum SPF 30 containing 2.30805 g active ingredient per 30 mL. The label highlights Bio-BoostRED Technology, Fermented Kefir, and Niacinamide, and indicates the product is fragrance-free, suitable for all skin types including sensitive skin, and dermatologist-tested. Manufactured by Shiseido Americas Corporation.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 120 emulsion containing 2.30805 g/30mL of Octinoxate as active sunscreen ingredient. The label includes the product name, SPF30, key features like Bio-BoostRED Technology, Fermented Kefir, and Niacinamide. It also shows the labeler as SHISEIDO AMERICAS CORPORATION and contains typical drug facts and directions for use.*

FDA Label Image

Principal Display Panel (30 mL Container Carton)

Packaging label for SHISEIDO REVITALESSENCE SKIN GLOW Foundation 30mL emulsion containing Octinoxate 6.9% as the active ingredient. The label features branding details such as SHISEIDO GINZA TOKYO, broad spectrum SPF30 sunscreen protection, Bio-BoostRED Technology, and ingredients like Fermented Kefir and Niacinamide. It is labeled for topical use and distributed by Shiseido Americas Corporation.*

* 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.