Luminosity Activation Day Edition Kit
Product Images NDC 83108-100

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Luminosity Activation Day Edition (NDC 83108-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rationale Group Pty Ltd, 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

Label (Label)

Luminosity Activation Day Edition kit by Rationale Group Pty Ltd, containing three 3 mL units. The label highlights Zinc Oxide as an active ingredient at 24%, used for sun protection. The packaging includes drug facts, directions, warnings, and a list of inactive ingredients. The product is identified as human OTC drug with 240 mg/mL strength and is distributed by Rationale USA LLC.*

FDA Label Image

Label2 (Label2)

Labels for RATIONALE skincare serums including The Light Crème 3mL with stylized orange "R" logo, The Serum 3mL with a yellow abstract logo, and The Tinted Serum SPF50+ 3mL with a green logo. All bottles are depicted as dropper bottles and state "Made in Australia" with distribution by RATIONALE USA LLC. Each label notes the product is a sample only and not for resale, with some text in English and Chinese.*

* 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.