Coco Eve Sunny Honey Highlighter Body Spf 50
Product Images NDC 68577-244

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Coco Eve Sunny Honey Highlighter Body Spf 50 (NDC 68577-244). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosmax Usa, 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

Package (Bottle)

COCO EVE SUNNY HONEY HIGHLIGHTER BODY SPF 50 in a 158 mL (5.87 fl oz) clear plastic cylindrical bottle with a shiny metallic pink pump cap. The label shows the product name in pink text, SPF 50 protection, and indicates it is a highlighter body sunscreen with ingredients like vitamin E and cacao extract. The bottle highlights water resistance for 40 minutes and broad spectrum UVA/UVB protection.*

FDA Label Image

Label (Label)

Drug Facts panel for COCO EVE SUNNY HONEY HIGHLIGHTER BODY SPF 50 sunscreen by COSMAX USA. The panel lists active ingredients (Homosalate 15%, Octocrylene 10%, Octisalate 5%, Avobenzone 3%) with their purpose as sunscreen. It includes uses, warnings, and directions for use. The text above promotes the product as a lightweight, serum-like sunscreen that nourishes and smooths skin with a tropical mango scent. Distributor information and a barcode are also visible.*

FDA Label Image

Label-2 (Label2)

This panel shows drug facts with directions for use, sun protection measures, a detailed list of inactive ingredients, other important information about product storage, and a contact phone number for questions. It includes instructions on applying the product before sun exposure, advises sun safety precautions, and lists various botanical and chemical inactive ingredients.*

* 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.