Pro Triple Protection Factor Broad Spectrum Spf 50 Sunscreen
Product Images NDC 67938-2075

2 FDA label images from Elizabeth Arden, Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Pro Triple Protection Factor Broad Spectrum Spf 50 Sunscreen (NDC 67938-2075). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Elizabeth Arden, Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Principal Display Panel (Bottle Label)

Principal Display Panel (Bottle Label)
Label for PRO TRIPLE PROTECTION FACTOR BROAD SPECTRUM SPF 50 SUNSCREEN lotion by Elizabeth Arden, Inc. The physical sunscreen has a universal tint and contains 1.7 fluid ounces (50 ml). Active ingredients titanium dioxide (6.1%) and zinc oxide (5.6%) are listed. The label includes usage instructions, warnings, and the distributor information from Elizabeth Arden, Inc., New York.*
FDA Label Image

Principal Display Panel (Carton Label)

Principal Display Panel (Carton Label)
Packaging label for PRO TRIPLE PROTECTION FACTOR BROAD SPECTRUM SPF 50 SUNSCREEN Lotion by ELIZABETH ARDEN, INC. The label shows the product name, broad spectrum SPF 50, a 1.7 FL. OZ. (50 ml) volume, and branding. It includes a detailed Drug Facts panel with active ingredients titanium dioxide 6.1% and zinc oxide 5.6% as sunscreens, usage directions, warnings, inactive ingredients, and storage instructions. The label design features a red top section and gray main panel with black and red text.*

* 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.