Iolite Gel
Product Images NDC 53045-135

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Iolite (NDC 53045-135). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dharma Research, 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

20201013 135 Revd

This is a warning label with important information about using an anesthetic gel with ingredients including Vitamin E and Xylitol. The gel should not be used for more than 7 days unless directed by a doctor. If certain symptoms such as gray or blue colored skin, headache, or dizziness occur, seek immediate medical attention. The label also warns against using the product if you have a history of allergies to certain anesthetics. If accidentally swallowed, seek medical help or contact a Poison Control Center.*

* 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.