Shiseido Synchro Skin Self-refreshing Foundation 530 Henna Emulsion
Product Images NDC 58411-510

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Shiseido Synchro Skin Self-refreshing Foundation 530 Henna (NDC 58411-510). 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 Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO SYNCHRO SKIN SELF-REFRESHING Foundation 440 Amber, an emulsion topical sunscreen with broad spectrum SPF 30. The label highlights active ingredients octinoxate 4.9% and titanium dioxide 1%, with 30 mL (1 FL.OZ.) volume. It is oil-free and produced by Shiseido Americas Corporation. The label includes drug facts, usage warnings, directions, inactive ingredients, and sun protection measures.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO SYNCHRO SKIN SELF-REFRESHING Foundation 440 Amber, a topical emulsion sunscreen with active ingredients Octinoxate 4.9% and Titanium Dioxide 1%. The label indicates oil-free, broad spectrum SPF 30 protection. The container size is 30 mL (1 FL. OZ.), distributed by SHISEIDO AMERICAS CORPORATION. The label includes drug facts, usage directions, warnings, inactive ingredients, and contact information.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO SYNCHRO SKIN SELF-REFRESHING Foundation 30mL emulsion with SPF 30 sunscreen. The label highlights active ingredients Octinoxate 4.9% and Titanium Dioxide 1%, displays directions for use, warnings, and inactive ingredients. Manufacturer indicated as Shiseido Americas Corporation.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO SYNCHRO SKIN SELF-REFRESHING Foundation 440 Amber, a topical emulsion sunscreen with broad spectrum SPF 30. The label includes active ingredients Octinoxate 4.9% and Titanium Dioxide 1%, with a volume of 30 mL (1 FL. OZ). It displays warnings, usage directions, inactive ingredients, and manufacturer information for Shiseido Americas Corporation.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO SYNCHRO SKIN SELF-REFRESHING Foundation 440 AMBER, an oil-free emulsion sunscreen with broad spectrum SPF 30. Contains active ingredients octinoxate 4.9% and titanium dioxide 1%. The label includes directions, warnings, inactive ingredients, and manufacturer information (Shiseido Americas Corporation). The container size is 30 mL (1 fl. oz).*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO SYNCHRO SKIN SELF-REFRESHING Foundation 440 Amber emulsion with broad spectrum SPF 30 sunscreen. Contains active ingredients Octinoxate 4.9% and Titanium Dioxide 1%, in a 30 mL (1 FL. OZ.) bottle. Labeler: SHISEIDO AMERICAS CORPORATION. The product is oil-free and designed for topical use with claims of weightless comfort and buildable coverage.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO SYNCHRO SKIN SELF-REFRESHING Foundation 440 Amber. The product is a 30 mL (1 FL. OZ.) topical emulsion with active ingredients Octinoxate 4.9% and Titanium Dioxide 1%, serving as a sunscreen with broad spectrum SPF 30. The label includes directions, warnings, inactive ingredients, manufacturer information (Shiseido Americas Corporation), and product features such as oil-free formula and dermatological testing.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO SYNCHRO SKIN SELF-REFRESHING Foundation 440 Amber, an oil-free emulsion sunscreen with broad spectrum SPF 30. The label highlights active ingredients octinoxate 4.9% and titanium dioxide 1%, with a net content of 30 mL (1 fl. oz.). Labeler is SHISEIDO AMERICAS CORPORATION. The design includes product warnings, directions, inactive ingredients, and company contact information.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO Synchro Skin Self-Refreshing Foundation 440 Amber, a topical emulsion sunscreen with active ingredients Octinoxate 4.9% and Titanium Dioxide 1%. The label indicates SPF 30 broad spectrum protection, oil-free formula, and a 30 mL (1 FL. OZ.) size. Manufactured by Shiseido Americas Corporation, the label includes directions, warnings, inactive ingredients, and product information emphasizing non-comedogenic properties and medium buildable coverage.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Packaging label for SHISEIDO Synchro Skin Self-Refreshing Foundation 440 Amber, a topical emulsion sunscreen with active ingredients octinoxate 4.9% and titanium dioxide 1%. The label indicates broad spectrum SPF 30, oil-free formulation, and a 30 mL (1 fl. oz.) container. Manufactured by Shiseido Americas Corporation, the label includes drug facts, warnings, directions, inactive ingredients, 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.