Cetaphil Sheer Mineral Face Liquid Sunscreen Spf 50 Lotion
Product Images NDC 0299-4110

2 FDA label images from Galderma Laboratories, L.p. · 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 Cetaphil Sheer Mineral Face Liquid Sunscreen Spf 50 (NDC 0299-4110). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Galderma Laboratories, L.p., 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

Cetaphil Sun Spf 50 Liq Bottlefront

Cetaphil Sun Spf 50 Liq  Bottlefront
Cetaphil Sheer Mineral Face Liquid Sunscreen SPF 50 lotion label showing the Cetaphil logo, SPF 50 sun protection, and product description emphasizing broad spectrum protection. The label specifies features like formulation for sensitive skin, microbiome gentle, water resistance for 80 minutes, and suitability for use under makeup, including vitamin E. The bottle size indicated is 1.7 FL OZ (50 mL).*
FDA Label Image

P55342 0 Cetaphil Sun Spf 50 Liquid Drops 1.7oz Carton

P55342 0 Cetaphil Sun Spf 50 Liquid Drops 1.7oz Carton
Packaging label for Cetaphil Sheer Mineral Face Liquid Sunscreen SPF 50 lotion by Galderma Laboratories, L.P. The front panel highlights broad spectrum SPF 50 protection with zinc oxide as the active ingredient (120 mg/mL). It is a 1.7 FL OZ (50 mL) cream noted for being formulated for sensitive skin, fragrance-free, paraben-free, mineral oil-free, and hypoallergenic. Drug Facts and usage instructions are detailed on the side panel.*

* 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.