Dior Backstage Glow-up Skin Tint Tinted Moisturizer Spf 20 2.5n Neutral Emulsion
Product Images NDC 61957-3706

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dior Backstage Glow-up Skin Tint Tinted Moisturizer Spf 20 2.5n Neutral (NDC 61957-3706). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Parfums Christian Dior, 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

Box7 (Box7)

Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2.5N Neutral by Parfums Christian Dior. The label shows a blue carton with product name and details, including 40 ml (1.3 FL OZ) volume, broad spectrum SPF 20, and active ingredients Octisalate 4.50% and Titanium dioxide 4.23%. Includes Drug Facts with usage, warnings, and directions for topical emulsion sunscreen.*

FDA Label Image

Inner Label7 (Inner Label7)

Label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 in shade 2.5N Neutral. The topical emulsion lists octisalate 4.50% and titanium dioxide 4.23% as active ingredients. The label indicates a 40 mL (1.3 fl oz) container made by Parfums Christian Dior in France, with instructions for external use only and a 12-month period after opening symbol.*

FDA Label Image

Outer Label7 (Outer Label7)

Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2.5N Neutral, a topical emulsion sunscreen product by Parfums Christian Dior. The blue box includes product branding, active ingredients Octisalate 4.50% and Titanium dioxide 4.23%, directions, warnings, and ingredient lists. The package size is 40 ml (1.3 FL.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.