Dior Backstage Glow-up Skin Tint Tinted Moisturizer Spf 20 3.5n Neutral Emulsion
Product Images NDC 61957-3710

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 3.5n Neutral (NDC 61957-3710). 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

Box11 (Box11)

Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 3.5N Neutral. The product is an emulsion topical sunscreen with active ingredients Octisalate (4.50%) and Titanium dioxide (4.23%). The label includes drug facts with uses, warnings, directions, and ingredients, and states a volume of 40 ml (1.3 FL.OZ). Labeler is Parfums Christian Dior, made in France, with barcode and product NDC 61957-3710 visible. The packaging is primarily blue with silver text.*

FDA Label Image

Inner Label11 (Inner Label11)

Label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 3.5N Neutral emulsion, topical use, by Parfums Christian Dior. The label shows active ingredients Octisalate 4.50% and Titanium dioxide 4.23%, volume 40 mL (1.3 FL. OZ), and usage instructions with warnings. The label is in both English and French, includes a 12M use period symbol, and product packaging dimensions.*

FDA Label Image

Outer Label11 (Outer Label11)

The packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 3.5N Neutral displays the brand and product name prominently on a blue background. It is a 40 ml topical emulsion sunscreen product by Parfums Christian Dior. The label includes active ingredients octisalate 4.50% and titanium dioxide 4.23%, along with detailed drug facts, directions, warnings, and inactive ingredients.*

* 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.