Minoxidil Aerosol, Foam
Product Images NDC 51672-2129

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Minoxidil (NDC 51672-2129). 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

Principal Display Panel (60 g Can Package)

Minoxidil For Women topical aerosol 5% (50 mg/g) foam for hair regrowth treatment by Sun Pharmaceutical Industries, Inc. The label features product details, usage directions, warnings, and active ingredients. The 60 g (2.11 oz) can is an unscented, once-a-day foam designed for topical application on the scalp. Packaging includes instructions for use, safety warnings, and manufacturer information.*

* 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.