Antifungal Foot Treatment
Product Images NDC 83004-016

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Antifungal Foot Treatment (NDC 83004-016). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rida Llc, 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

Image Description (Label1)

Antifungal Foot Treatment packaging label by Rida LLC features a dark green and black color scheme. The front displays the product name, antifungal foot gel with tea tree oil, and mentions prescription strength butenafine hydrochloride 1%. The label highlights a no-touch applicator and fast relief from athlete's foot symptoms including itching, burning, cracking, and scaling. The net weight is 20g (0.70 oz). The side panel includes drug facts, directions, warnings, and inactive ingredients. The packaging also features icons for 12-month shelf life, recycling, and cruelty-free status.*

FDA Label Image

Image Description (Label2)

Label for Antifungal Foot Gel, prescription strength, 20g (0.70 oz) tube by Rida LLC. The label highlights fast relief of athlete's foot symptoms such as itching, burning, cracking, and scaling. It features a triple action formula meant to soothe discomfort, relieve symptoms, and provide fast-acting relief. Manufactured by Terramed LLC, San Diego, CA.*

* 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.