Iolite Gel
Product Images NDC 53045-138

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Iolite (NDC 53045-138). 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.

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FDA Label Image

20201013 138 Revd

20201013 138 Revd
This is a description of a product that is an ANESTHETIC GEL. It contains Vitamin E and Xylitol. It is suggested to use for temporary relief of lesions in the mouth. The use of this product may cause methemoglobinemia, which must be treated promptly because it reduces the amount of oxygen carried in the blood. If suffering from pale, gray, or blue-colored skin (cyanosis), headache, rapid heart rate, shortness of breath, dizziness, or lightheadedness, stop using immediately and seek medical help. Do not use this product if you are allergic to local anesthetics. Do not use for more than seven days, unless directed by a dentist or doctor. If sore mouth symptoms do not improve in seven days, see your dentist or doctor promptly. If more than the recommended dose is accidentally swallowed, contact a Poison Control Center right away.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.