Glamtox Active Daily Moisturizing Sunscreen
Product Images NDC 52456-018

3 FDA label images from Rodial, Ltd. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Glamtox Active Daily Moisturizing Sunscreen (NDC 52456-018). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rodial, 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.

Product Images & Figures Index

FDA Label Image

Glamtoxbox (Box)

Glamtoxbox (Box)
Outer packaging carton for GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN by Rodial, Ltd. The label shows the product name, SPF 18 designation, product volume of 1.7 fl oz (50 mL), and highlights ingredients such as pomegranate elagic tannin. The Rodial logo and website URL are also visible.*
FDA Label Image

Glamtoxbottle (Glamtox Bottle)

Glamtoxbottle (Glamtox Bottle)
Label for Glamtox Active Daily Moisturizing Sunscreen Lotion SPF 18 by Rodial Ltd. The product volume is 1.7 fl oz (50 mL). It highlights protection with pomegranate ellagic tannin cell protection. Directions state to apply liberally before sun exposure and as needed, with specific instructions for use.*
FDA Label Image

Glamtoxdrugpanel (Glamtox Panel)

Glamtoxdrugpanel (Glamtox Panel)
Drug Facts panel of GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN by Rodial, Ltd., listing active ingredients homosolate 3%, octinoxate 8%, and oxybenzone 2% as sunscreens. The panel includes sections on uses, warnings, directions, and inactive ingredients, providing detailed information on application, safety precautions, and product composition.*

* 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.