Dior Backstage Glow-up Skin Tint Tinted Moisturizer Spf 20 4n Neutral Emulsion
Product Images NDC 61957-3715

View Photos of Packaging, Regulatory Labels, and Product Appearance

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 4n Neutral (NDC 61957-3715). 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

Box16 (Box16)

Box16 (Box16)
Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 4N Neutral, a topical emulsion sunscreen by Parfums Christian Dior. The 40 ml (1.3 FL. OZ) container states broad spectrum SPF 20 protection and highlights active ingredients Octisalate 4.50% and Titanium dioxide 4.23%. The label includes usage, warnings, directions, inactive ingredient list, and recycling information.*
FDA Label Image

Inner Label16 (Inner Label16)

Inner Label16 (Inner Label16)
Label design for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 4N Neutral emulsion. The oval-shaped label includes product name, active ingredients Octisalate 4.50% and Titanium dioxide 4.23%, usage warnings, volume of 40 mL (1.3 FL OZ), and manufacturer information Parfums Christian Dior, made in France. Additional details include instructions to shake well and a 12-month shelf life symbol.*
FDA Label Image

Outer Label16 (Outer Label16)

Outer Label16 (Outer Label16)
Packaging label for Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 4N Neutral. The product is a 40 ml topical emulsion sunscreen and skin beautifier with broad spectrum SPF 20. Labeler is Parfums Christian Dior. The label includes active ingredients Octisalate 4.50% and Titanium dioxide 4.23%, along with usage directions, warnings, and inactive ingredients. It includes drug facts and a barcode.*

* 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.