Dior Backstage Glow-up Skin Tint Tinted Moisturizer Spf 20 6n Neutral Emulsion
Product Images NDC 61957-3720

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 6n Neutral (NDC 61957-3720). 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

Box21 (Box21)

Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 6N Neutral, an emulsion topical product by Parfums Christian Dior. The 40 ml (1.3 fl oz) package features Drug Facts, including active ingredients Octisalate 4.50% and Titanium Dioxide 1.41%. Label includes directions for use, warnings, inactive ingredients, and SPF 20 broad spectrum sunscreen information.*

FDA Label Image

Inner Label21 (Inner Label21)

Label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 6N Neutral, an emulsion topical product by Parfums Christian Dior. The label includes active ingredients Octisalate 4.50% and Titanium dioxide 1.41%. The product is presented as a 40 ml (1.3 FL.OZ) container made in France. Directions and warnings for external use are also printed on the label.*

FDA Label Image

Outer Label21 (Outer Label21)

Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 6N Neutral by Parfums Christian Dior. The label shows a 40 ml (1.3 FL.OZ) emulsion topical product containing active ingredients Octisalate 4.50% and Titanium Dioxide 1.41%, indicated as sunscreen. The carton is blue with large DIOR branding and includes Drug Facts with uses, warnings, directions, and ingredient listings.*

* 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.