Dapsone Gel
Product Images NDC 51672-1388

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dapsone (NDC 51672-1388). 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)

FDA Label Image

Principal Display Panel (60 g Bottle Carton)

Principal Display Panel (60 g Bottle Carton)
This is a warning label for Dapsone Gel. Each gram contains Dapsone 175%, within a gel of carbomer homopolymer type G, diethylene glycol monoethyl ether, mineral oil, methylparaben, polyoxyl 20 cetostearyl ether, purified water, sodium hydroxide, and sorbitan monodleate. It is for topical use only and the dosage is to be applied once daily. The label warns to keep it out of reach of children and to not ingest it as it is not for oral, ophthalmic, or intravaginal use. The product should be stored at 20-25°C and not be frozen. The flap of the carton contains information on the lot number and expiry date. This product is distributed by Taro Pharmaceuticals USA.*

* 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.