Barielle Professional Maximum Strength Fungus Rx Antifungal Pro
Product Images NDC 42593-001

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Barielle Professional Maximum Strength Fungus Rx Antifungal Pro (NDC 42593-001). 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

Barielle Professional Pro Fungus Rx Inner Package 1 (Barielleprofessionalprofungusrx Innerpackage1)

Label for Barielle Professional Maximum Strength Fungus Rx Antifungal PRO antifungal solution, 30 ml (1 fl oz). The label highlights the product name, strength, and dosage form, and states distribution by Fisk Industries from Orangeburg, NY, USA. The active ingredient listed is Tolnaftate 1.0%, and the Drug Facts panel indicates it is for external use only to treat athlete's foot and related symptoms.*

FDA Label Image

Barielle Professional Pro Fungus Rx Inner Package 2 (Barielleprofessionalprofungusrx Innerpackage2)

The image shows a text panel with directions for use, other information, and a list of inactive ingredients for Barielle Professional Maximum Strength Fungus Rx Antifungal PRO by Fisk Industries. Directions include hygiene tips and application frequency. Other information provides contact details for reporting adverse events. The inactive ingredients list various chemicals and extracts used in the product.*

FDA Label Image

Barielle Professional Pro Fungus Rx Outer Package 1 (Barielleprofessionalprofungusrx Outerpackage1)

Drug Facts panel for an antifungal product containing Tolnaftate 1.0% as the active ingredient. The panel details uses for treating athlete's foot, warnings for external use only, directions for application, and inactive ingredients list including water, PEG-8, and aloe extract. Contact information for Fisk Industries, Inc. is also provided.*

FDA Label Image

Barielle Professional Pro Fungus Rx Outer Package 2 (Barielleprofessionalprofungusrx Outerpackage2)

Packaging label for Barielle Professional Maximum Strength Fungus Rx Antifungal PRO solution. The label features a blue gradient background with white and gray text, highlighting the product name and antifungal function. The solution volume is 30 ml (1 Fl. Oz. U.S.). The label includes both English and French text and is from Fisk Industries.*

FDA Label Image

Barielle Professional Pro Fungus Rx Outer Package 3 (Barielleprofessionalprofungusrx Outerpackage3)

Label for Barielle Professional Maximum Strength Fungus Rx Antifungal PRO, an antifungal solution in a 30 ml (1 fl oz) container. The label highlights the product's maximum strength and its use as an antifungal that kills germs causing fungal infections. It is distributed by Fisk Industries and made in the USA, with manufacturing details referring to Biorius SPRL in Belgium.*

FDA Label Image

Barielle Professional Pro Fungus Rx Outer Package 4 (Barielleprofessionalprofungusrx Outerpackage4)

Label for Barielle Professional Maximum Strength Fungus Rx Antifungal PRO solution in a 30 ml (1 fl. oz.) bottle. The label displays the product name in Spanish as Máxima Potencia and indicates it is an antifungal solution. The label features a gradient blue to white background with bold text and is labeled with part number 0326FC.*

* 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.