E L F Camo Semi Matte Cc Spf 30 Light 210 N Cream
Product Images NDC 76354-513

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 E L F Camo Semi Matte Cc Spf 30 Light 210 N (NDC 76354-513). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by E.l.f. Cosmetics, 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.

FDA Label Image

Inner Package5 (Inner Package5)

Inner Package5 (Inner Package5)
Packaging label for e.l.f. Cosmetics e.l.f Camo Semi Matte CC SPF 30 Light 210 N cream. The front includes the brand name e.l.f., product name CAMO CC CREAM, claims of full coverage, long-lasting semi-matte finish, and Broad Spectrum SPF 30 sunscreen. The back shows directions for use and active ingredients including zinc oxide (6.3%), titanium dioxide (6%), homosalate (5%), octisalate (4.5%), and octocrylene (3%). The label also states external topical use and cautions.*
FDA Label Image

Outer Package4 (Outer Package4)

Outer Package4 (Outer Package4)
Packaging label for e.l.f. Cosmetics Inc.'s e l f Camo Semi Matte CC SPF 30 Light 210 N cream. The label shows a 1 oz (30 g) tube of full coverage, long-lasting semi-matte finish color-correcting cream with broad spectrum SPF 30 sunscreen. It highlights the neutral beige undertones shade, and features product claims and Drug Facts including active ingredients Zinc Oxide 6.3%, Titanium Dioxide 6%, Homosalate 5%, Octisalate 4.5%, and Octocrylene 3%, all as sunscreens. The label also carries vegan, cruelty-free, and fair trade certifications.*

* 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.