Derma Soleil Natural Sunblock Spf 30
Product Images NDC 69711-305

2 FDA label images from Derma Soleil · 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 Derma Soleil Natural Sunblock Spf 30 (NDC 69711-305). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Derma Soleil, 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

240 mL Tube (69711 306 Ds Adult Spf30 240ml Label)

240 mL Tube (69711 306   Ds Adult Spf30 240ml Label)
Derma Soleil Natural Sunblock Broad Spectrum SPF 30 sunscreen in an 8.0 fl. oz (240 mL) container. The label highlights moisturizing ingredients including Vitamins A, C, E, and Aloe, and states the product is water-resistant for 40 minutes, PABA-free, and suitable for all skin types. The back label lists active ingredients Octocrylene 4%, Octyl Methoxycinnamate 7.5%, Octyl Salicylate 4%, and Oxybenzone 5%, usage directions, warnings, inactive ingredients, and contact information for the labeler Derma Soleil.*
FDA Label Image

120 mL Tube (69711 306 Ds Adult Spf30 120ml Label)

120 mL Tube (69711 306  Ds Adult Spf30 120ml Label)
Derma Soleil Natural Sunblock Broad Spectrum SPF 30 lotion in a 120 mL (4.0 fl. oz.) package. The label highlights moisturizing with vitamins A, C, E, and Aloe, UVA/UVB protection, water resistance for 40 minutes, and PABA free formulation. Suitable for all skin types. Distributed by Biological Health Group, made in Canada. The back panel includes drug facts, uses, warnings, directions, inactive ingredients, and contact 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.