Dapsone
Product Images NDC 51672-5307

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dapsone (NDC 51672-5307). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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

Chemical Structure (Dapsone 01)

Chemical structure of Dapsone, showing two benzene rings connected by a sulfone (SO2) group, each benzene ring substituted with an amino (NH2) group.*

FDA Label Image

60 G Carton Label (Dapsone 02)

Packaging label for Dapsone Gel 7.5%, 60 g, produced by Sun Pharmaceutical Industries, Inc. The label shows directions for topical use only, dosing instructions to apply once daily, a warning to keep out of reach of children, and storage conditions. The label also includes manufacturer and distributor information, a barcode, and NDC 51672-5307-3.*

FDA Label Image

60 G Pump Label (Dapsone 03)

Dapsone Gel 7.5% topical gel, 60 g package, with labeler Taro Pharmaceuticals U.S.A., Inc. The label indicates it is for topical use only and includes warnings to keep out of reach of children and storage instructions. The product is Rx only and manufactured by DPT Laboratories, Ltd., San Antonio, TX.*

FDA Label Image

90g Carton Label (Dapsone 04)

Dapsone Gel 7.5% packaging label showing a 90 g tube. The label indicates topical use only and includes storage information. Manufactured by DPT Laboratories, Ltd. and distributed by Taro Pharmaceuticals U.S.A., Inc. The label features a barcode and reiterates that the product is prescription-only.*

FDA Label Image

90 G Pump Label (Dapsone 05)

Dapsone Gel 7.5% topical gel in a 90 g package by Sun Pharmaceutical Industries, Inc. The label states it is for topical use only and includes warnings, storage instructions, and inactive ingredients. The NDC 51672-5307 is visible, along with distributor information for Taro Pharmaceuticals U.S.A., 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.