Beet The Sun Lightweight Sunscreen Broad Spectrum Spf 40 Pa Lotion
Product Images NDC 83493-150

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 Beet The Sun Lightweight Sunscreen Broad Spectrum Spf 40 Pa (NDC 83493-150). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Krave Beauty, 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)
Label for Beet The Sun Lightweight Sunscreen Broad Spectrum SPF 40 PA+++ lotion by Krave Beauty, LLC. The front highlights the product name, SPF 40 strength, and key ingredients beetroot, hyaluronic acid, and vitamin E in a 1.7 fluid ounce (50 mL) size. The back includes product use instructions, active ingredients (Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 3%), and sustainability claims such as 90% post-consumer recycled plastic tube and various eco-certifications.*
FDA Label Image

Outer Package (Outer Package)

Outer Package (Outer Package)
The image shows the Drug Facts panel and detailed product information for Beet The Sun Lightweight Sunscreen Broad Spectrum SPF 40 PA+++, a topical lotion by Krave Beauty, LLC. It lists active ingredients Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 3% with their purposes as sunscreens. It includes uses, warnings, directions, inactive ingredients, and a product description highlighting its antioxidant-rich beetroot extract formula. The label also features social media handles, recycling and certification logos, bottle size (1.7 fl. oz./50 mL), and a barcode.*

* 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.