Dior Backstage Glow-up Skin Tint Tinted Moisturizer Spf 20 0n Neutral Emulsion
Product Images NDC 61957-3701

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 0n Neutral (NDC 61957-3701). 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

Box2 (Box2)

Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 0N Neutral, a topical emulsion sunscreen containing octisalate 4.50% and titanium dioxide 4.23%. The 40 ml (1.3 fl oz) box is royal blue with silver text, featuring brand and product name, broad spectrum SPF 20, and usage directions. Manufactured by Parfums Christian Dior in France.*

FDA Label Image

Inner Label2 (Inner Label2)

Label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 0N Neutral emulsion by Parfums Christian Dior. The label shows the product name, active ingredients Octisalate 4.50% and Titanium dioxide 4.23%, usage warnings, volume of 40 mL (1.3 FL OZ), manufacturing origin in France, and directions to shake well and apply 15 minutes before sun exposure.*

FDA Label Image

Outer Label2 (Outer Label2)

Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 0N Neutral, a topical emulsion sunscreen by Parfums Christian Dior. The label features the product name, volume of 40 ml (1.3 fl. oz), broad spectrum SPF 20, active ingredients octisalate 4.50% and titanium dioxide 4.23%, Drug Facts, and various inactive ingredients. The packaging is predominantly blue with silver and blue text and includes a barcode and manufacture details.*

* 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.