Dreambeam Sunscreen Lotion
Product Images NDC 82554-102

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dreambeam Sunscreen (NDC 82554-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kosas Cosmetics, 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

Outer (Dreambeam Inactive)

This drug facts panel lists the inactive ingredients of DreamBeam Sunscreen lotion, which include water, caprylic/capric triglyceride, butyloctyl salicylate, various glyceryl esters, silica, botanical extracts, sodium hyaluronate, vitamin E derivative, and colorants such as titanium dioxide and iron oxides.*

FDA Label Image

Tube (Dreambeam Primary)

The image shows the front and back of a pink bottle of DreamBeam Sunscreen Lotion by Kosas Cosmetics, LLC. It contains Sunscreen Zinc Oxide at 21.7 g/100mL with Broad Spectrum SPF 40 and is water resistant for 80 minutes. The back lists skincare ingredients like mineral SPF, peptides, ceramides, allantoin, and hyaluronic acid, indicating it can be worn alone or as a makeup base. The bottle size is 40 mL (1.36 fl oz).*

FDA Label Image

Outer (Dreambeam Sec)

The DreamBeam Sunscreen lotion packaging label from Kosas Cosmetics, LLC. It contains Zinc Oxide 21.7 g/100mL as the active ingredient. The label highlights a broad spectrum SPF 40 PA++++ that is water resistant for 80 minutes. The lotion comes in a 40 mL (1.35 fl. oz.) bottle and is described as a mineral sunscreen that moisturizes and smooths, suitable for sensitive skin, hypoallergenic, non-comedogenic, vegan, and fragrance-free.*

* 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.