Sun Bum Tinted Sunscreen Lip Balm Broad Spectrum Spf 15 - Bonfire Carded Stick
Product Images NDC 69039-737

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sun Bum Tinted Sunscreen Lip Balm Broad Spectrum Spf 15 - Bonfire Carded (NDC 69039-737). 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

Primary Artwork (Sb Tinted Lipbalm Blister Bonfire R1v1 444107)

Packaging label for Sun Bum Tinted Sunscreen Lip Balm Broad Spectrum SPF 15 in the Bonfire shade, presented as a single blister pack. The label features the Sun Bum logo with a stylized monkey face, product name, and sunscreen information. It lists the active ingredients Homosalate, Octisalate, Octocrylene, and Zinc Oxide. The labeler is Sun Bum, LLC, and the package net weight is 0.15 oz (4.25 g). The design uses Pantone colors 704 U, 2322 C, and 601 C.*

FDA Label Image

Primary Artwork (Sb Tinted Lipbalm Bonfire R1v1 444106)

Label for Sun Bum Tinted Sunscreen Lip Balm Broad Spectrum SPF 15 - Bonfire. The label features the Sun Bum logo with the product name and variant "Bonfire". It includes drug facts with active ingredients: Homosalate 10%, Octisalate 5%, Octocrylene 3%, Zinc Oxide 2.6%. The label also mentions product uses, warnings, directions, and color callouts for printing. The label highlights key properties such as gluten-free, silicone-free, paraben-free, hypoallergenic, and oxybenzone-free. Net weight is 0.15 oz (4.25 g). The product is manufactured and distributed by Sun Bum, LLC in the USA.*

* 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.