Hand Screen Broad Spectrum Sunscreen Spf 40 Lotion
Product Images NDC 75936-151

2 FDA label images from Supergoop, 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 Hand Screen Broad Spectrum Sunscreen Spf 40 (NDC 75936-151). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Supergoop, 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

Carton (08.17.22 Handscreen Spf 40 1 Fl. Oz Carton Ol Page 1)

Carton (08.17.22 Handscreen Spf 40 1 Fl. Oz Carton Ol Page 1)
Packaging label layout for Hand Screen Broad Spectrum Sunscreen SPF 40 lotion by Supergoop, LLC. The label includes product branding, SPF 40 designation, and mentions active ingredients Avobenzone 3%, Octisalate 5%, and Octocrylene 10%. It lists product attributes like dermatologist-tested, non-irritating, reef-friendly, cruelty-free, and vegan. The label features application directions, usage warnings, and a barcode. The design is primarily yellow with blue, gray, and silver accents.*
FDA Label Image

Bottom (03.24.22 Handscreen Spf 40 6.76 Fl. Oz Ol)

Bottom (03.24.22 Handscreen Spf 40 6.76 Fl. Oz Ol)
Technical drawing of a cylindrical container for Supergoop! Hand Screen Broad Spectrum Sunscreen SPF 40 lotion. The drawing includes detailed top and side views with dimensions of diameters and heights. The label design displays product name, SPF 40, broad spectrum sunscreen designation, volume of 6.76 fl. oz. (200 mL), and drug facts. Color codes and manufacturer information for Supergoop, LLC in San Antonio, TX, are also shown.*

* 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.