Doterra Sun Stick
Product Images NDC 71630-175

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 Doterra Sun (NDC 71630-175). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Doterra International, 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

Stick Carton (Sun And Face Body Stick Carton V2)

Stick Carton (Sun And Face Body Stick Carton V2)
The doTERRA Sun Face + Body SPF 40 mineral sunscreen stick packaging label features zinc oxide 17.6% as the active ingredient. The label includes branding with 'doTERRA sun' and highlights broad spectrum SPF 40 protection. Net weight is 1.75 oz / 50 g. Manufacturer is doTERRA International, LLC. The label also provides drug facts, usage directions, warnings, inactive ingredients, and marketing claims emphasizing nourishment, environmental consciousness, and a clean formula free from oxybenzone, parabens, and phthalates.*
FDA Label Image

Tube Direct Stick Label (Sun And Face Body Tube Stick V2)

Tube Direct Stick Label (Sun And Face Body Tube Stick V2)
doTERRA Sun Face + Body Mineral Sunscreen Stick SPF 40 contains 17.6% zinc oxide as the active ingredient for topical sun protection. This 1.75 oz (50 g) broad spectrum sunscreen stick is manufactured by doTERRA International, LLC. The orange label highlights its mineral-based formulation, reef-safe and vegan-friendly features, and absence of parabens, phthalates, oxybenzone, benzene, and synthetic fragrances.*

* 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.