Dolce And Gabbana Blueberry Nutri Tint Spf 20 24n Medium Emulsion
Product Images NDC 84003-064

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 Dolce And Gabbana Blueberry Nutri Tint Spf 20 24n Medium (NDC 84003-064). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dolce & Gabbana Beauty S.r.l, 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

Label (Label 1)

Label (Label 1)
Dolce and Gabbana Blueberry Nutri Tint SPF 20 24N Medium emulsion sunscreen packaged by Dolce & Gabbana Beauty S.R.L. The label highlights 67 mg/mL Zinc Oxide as the active ingredient, with a net content of 1.01 fl. oz. (30ml). The packaging emphasizes hydration with glyceryl glucoside, blueberry extract, and broad spectrum SPF 20 protection, made in Italy. Drug facts and usage instructions are also detailed on the label.*
FDA Label Image

Inner Label (Label 2)

Inner Label (Label 2)
Packaging label for Dolce and Gabbana Blueberry Nutri Tint SPF 20 24N Medium in a 1.01 fl oz (30 ml) emulsion container. The label shows the Dolce & Gabbana logo, product name, and claims such as Hydra-Glow & Fresh Skin Tint with sunscreen broad spectrum SPF 20. Distributed by Dolce & Gabbana Beauty S.R.L, made in Italy.*
FDA Label Image

Label (Label)

Label (Label)
The packaging label for Dolce and Gabbana Blueberry Nutri Tint SPF 20 24N Medium shows a brown carton with black text. It features the brand name Dolce & Gabbana prominently, along with product details like "Blueberry Nutri-Tint" and "Hydra-Glow & Fresh Skin Tint Sunscreen Broad Spectrum SPF 20." The label states the product is made in Italy and contains 1.01 fl oz (30 mL). Active ingredient Zinc Oxide 6.7% is listed under Drug Facts. The label also includes usage, warnings, directions, and inactive ingredients, plus barcodes and regulatory information.*

* 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.