Jafra Royal Luna Bright Kit
Product Images NDC 68828-285

2 FDA label images from Jafra Cosmetics International Inc · 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 Jafra Royal Luna Bright Kit (NDC 68828-285). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jafra Cosmetics International Inc, 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

Luna Bright Kit Front (Lunabrightminitubesusa 1)

Luna Bright Kit Front (Lunabrightminitubesusa 1)
Packaging label for Jafra Royal Luna Bright Kit by JAFRA COSMETICS INTERNATIONAL INC. The label features a close-up image of a woman's face and includes product details for four samples: Refining Gel Cleanser, Brightening Hydrogel Moisturizer, Brightening Serum Concentrate, and Brightening Daily Protector Broad Spectrum SPF 30, each 7.5 ml (0.25 FL OZ). The total content is 30 ml (1 FL OZ US). The label highlights the use of exclusive Royal Jelly RJx, with ingredient lists and usage instructions for the Brightening Serum Concentrate and Brightening Hydrogel Moisturizer.*
FDA Label Image

Luna Bright Kit Back (Lunabrightminitubesusa 2)

Luna Bright Kit Back (Lunabrightminitubesusa 2)
Drug Facts panel for Jafra Royal Luna Bright Kit includes active sunscreen ingredients Avobenzone 3%, Homosalate 10%, Octisalate 5%, and Octocrylene 7%, with directions for use and warnings. It also lists extensive inactive ingredients and usage instructions for the Refining Gel Cleanser. Additional product care information notes protection from excessive heat and sun exposure.*

* 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.