Fungifoam Aerosol, Foam
Product Images NDC 49406-004

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fungifoam (NDC 49406-004). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Tetra Corporation, 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

Tubebox (Tubebox)

Drug Facts for FungiFoam antifungal aerosol foam, containing Tolnaftate 1% topical antifungal. The panel includes active ingredient, uses for treating athlete's foot and ringworm, warnings, directions for use, inactive ingredients, and storage instructions. Directions emphasize cleaning and drying the foot, applying foam twice daily, and precautions for children. Additional information covers product claims, manufacturer, and contact details.*

FDA Label Image

Tubelabel (Tubelabel)

FungiFoam antifungal aerosol foam label containing tolnaftate 1% at 10 mg/mL strength. The label highlights use for athlete's foot and ringworm relief, directions for topical application, warnings about external use and child safety, and a list of inactive ingredients. Manufactured by The Tetra Corporation, Eaton Rapids, MI. NDC 49406-004.*

FDA Label Image

Box (Box)

FungiFoam antifungal aerosol foam with Tolnaftate 1% strength, topical use. This 2.5 fl oz (75 ml) package by The Tetra Corporation is labeled for treating athlete's foot and ringworm. The label highlights directions, warnings, inactive ingredients, and usage steps, emphasizing treatment and prevention of athlete's foot. The product is sold by prescription only.*

FDA Label Image

Label (Label)

Drug Facts panel for FungiFoam 1% Tolnaftate antifungal foam. It includes active ingredient and purpose, uses for athlete's foot and ringworm, warnings about external use and children under 2 years, detailed directions for use, storage instructions at room temperature (25°C), and a list of inactive ingredients. Label indicates it is dispensed only by physicians and manufactured by The Tetra Corporation.*

* 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.