Derman Antifungal Cream
Product Images NDC 54312-125

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Derman Antifungal (NDC 54312-125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Compania Internacional De Comercio, S.a.p.i De C.v., 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 Package3

Derman Antifungal Cream packaging label contains 1.76 oz (50 g). It specifies active ingredients Undecylenic Acid 5% and Zinc Undecylenate 18%, for topical use in athlete's foot treatment. The label notes usage directions, warnings, inactive ingredients, manufacturer (Taisho Pharmaceutical California), and that the product is made in Mexico. The design includes a brown and yellow color scheme with red accents and footprints graphic.*

FDA Label Image

Inner Package4

Derman Antifungal Cream label showing active ingredients undecylenic acid 5% and zinc undecylenate 18%. The 50 g (1.76 oz) topical cream is indicated for athlete's foot treatment. Label includes directions, warnings for external use only, and manufacturer details from Mexico. Distributed by Taisho Pharmaceutical California, Inc.*

FDA Label Image

Label

Derman Antifungal cream containing 5% Undecylenic acid and 18% Zinc undecylenate for topical use. The package indicates a net weight of 0.88 oz (25 g) and specifies use for the treatment of athlete's foot. Manufactured by Farmaqro, S.A. de C.V. in Mexico and distributed by Taisho Pharmaceutical California, Inc. The label includes warnings, directions, and inactive ingredients, with clear branding and regulatory information.*

FDA Label Image

Label2 (Label2)

Derman Antifungal cream containing undecylenic acid and zinc undecylenate is shown in a 25 g (0.88 oz) tube for topical use. The label highlights its antifungal purpose targeted for athlete's foot treatment. It lists active ingredients as undecylenic acid 5% and zinc undecylenate 18%. The product is manufactured by Farmaqro, S.A. de C.V. and distributed by Taisho Pharmaceutical California, Inc., with labeling in English and Spanish.*

FDA Label Image

Label3

Derman Antifungal Cream label featuring active ingredients Undecylenic acid 5% and Zinc undecylenate 18%. The cream is indicated for topical treatment of athlete's foot with a net weight of 0.88 oz (25 g). Distributed by Taisho Pharmaceutical California Inc. The label includes drug facts, warnings, directions, and a barcode.*

FDA Label Image

Label4

Derman Antifungal Cream topical product label showing active ingredients Undecylenic Acid 5% and Zinc Undecylenate 18%. It is packaged as a 0.88 oz (25 g) tube for athlete's foot treatment. Label includes directions, warnings, inactive ingredients, and states the product is manufactured in Mexico and distributed by Taisho Pharmaceutical California.*

FDA Label Image

Outer Package3

Derman Antifungal Cream, containing Undecylenic Acid 5% and Zinc Undecylenate 18%, presented in a 1.76 oz (50 g) tube. The label states it is for the treatment of athlete's foot and notes inactive ingredients such as cetyl alcohol, glycerin, and various glycols. Manufactured by FARMAQRO, S.A. DE C.V. in Mexico and distributed by Taisho Pharmaceutical California, Inc. The packaging includes usage directions, warnings, and a barcode.*

FDA Label Image

Outer Package4

Packaging label for Derman Antifungal Cream containing Undecylenic Acid 5% and Zinc Undecylenate 18%. This topical antifungal cream is for the treatment of athlete's foot. The net weight is 1.76 oz (50 g). The label shows the brand name Derman prominently along with usage instructions, warnings, inactive ingredients, and distributor information. It is made in Mexico and distributed by Taisho Pharmaceutical California Inc.*

* 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.