Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 351 Liquid
Product Images NDC 68828-324

View Photos of 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 Jafra Always Long Wear Foundation Broad Spectrum Spf 15 Sunscreen 351 (NDC 68828-324). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Distribuidora Comercial Jafra, S.a. De C.v., 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

Image Description (Image 1)

Image Description (Image 1)
Packaging label artwork for JAFRA ALWAYS Long Wear Foundation Broad Spectrum SPF 15 Sunscreen in liquid form. The label includes the product name, active ingredients (Homosalate, Octisalate, Zinc Oxide), net weight of 30g (1.05 oz), and directions, warnings, and inactive ingredients sections. The labeler is Distribuidora Comercial Jafra, S.A. de C.V. The label design includes placement instructions and shade name listing area, with various shade/formula numbers referenced for US distribution only.*
FDA Label Image

Image Description (Image 2)

Image Description (Image 2)
Packaging label for JAFRA ALWAYS Long Wear Foundation Broad Spectrum SPF 15 Sunscreen 351, a 30 g (1.05 oz) topical liquid product. The label includes branding, active ingredients (Homosalate 4.25%, Octisalate 4.75%, Zinc Oxide 6.75%), usage directions, warnings, inactive ingredients, and manufacturer information (Distribuidora Comercial Jafra, S.A. de C.V.). It details full coverage and 24-hour wear claims and displays drug facts and storage instructions.*

* 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.