Sun Bum Daily Mineral Sunscreen Moisturizer Spf30
Product Images NDC 69039-635

2 FDA label images from Sun Bum Llc · 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 Sun Bum Daily Mineral Sunscreen Moisturizer Spf30 (NDC 69039-635). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Bum Llc, 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 Package (Inner Package)

Inner Package (Inner Package)
The image shows the Drug Facts panel for Sun Bum Daily Sunscreen Moisturizer with Broad Spectrum SPF 30, water-resistant for 80 minutes. It lists active sunscreen ingredients—Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 10%—their purpose, uses, warnings, directions for application, and sun protection measures. The label includes manufacturer information for Sun Bum, LLC, recycling instructions, and a cruelty-free logo.*
FDA Label Image

Outer Package (Outer Package)

Outer Package (Outer Package)
The image shows the flattened carton packaging for Sun Bum Daily Mineral Sunscreen Moisturizer SPF 30 in a 1.7 FL OZ (50 mL) size. The front panel features the Sun Bum logo with an illustration of a person sitting on a yellow beach ball. The label notes broad spectrum SPF 30 and water resistance for 80 minutes, enriched with banana, wild rosella, and niacinamide. The back panel includes Drug Facts with active ingredients Avobenzone 3%, Homosalate 10%, Octisalate 5%, and Octocrylene 10%, usage instructions, warnings, directions, and inactive ingredients. The labeler is Sun Bum LLC, and the product barcode and contact information are also visible.*

* 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.