Barielle Fungus Rx Maximum Strength Anti-fungal
Product Images NDC 42593-002

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Barielle Fungus Rx Maximum Strength Anti-fungal (NDC 42593-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fisk Industries, 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

Inner Package 1 (Innerpackage1)

Drug Facts panel for Barielle Fungus Rx Maximum Strength Anti-Fungal Solution with active ingredient Tolnaftate 1%. It lists the purpose as an antifungal, and the uses include curing and preventing most athlete's foot symptoms. Warnings cover accidental ingestion, use halting in case of irritation, and keeping out of reach of children under 2 years. The panel advises external use only and to seek medical care if necessary.*

FDA Label Image

Inner Package 2 (Innerpackage2)

The image shows the back side (peel back) of a Barielle Fungus Rx Maximum Strength Anti-Fungal product label. It includes directions for use to prevent athlete's foot, other information on reporting serious adverse events to Fisk Industries, and a list of inactive ingredients such as water, PEG-8, Cetearyl Alcohol, and others. The phrase 'Stop Peeling' is also visible at the bottom.*

* 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.