Minoxidil Topical Solution 2% Solution
Product Images NDC 51672-2152

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Minoxidil Topical Solution 2% (NDC 51672-2152). 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.

Product Images & Figures Index

FDA Label Image

Carton Label (Carton Label)

Carton Label (Carton Label)
This is a description of a Women's Minoxidil Topical Solution USP 2%, a hair regrowth treatment. It contains detailed drug facts, usage instructions, and warnings. The solution is designed for women experiencing hair thinning or loss on the scalp. The product has been clinically proven to regrow hair in women and should be applied twice a day directly on the affected scalp area. It takes at least 4 months of regular use to see results. The solution is alcohol-based and includes inactive ingredients like propylene glycol and water. Users are advised to avoid contact with eyes, not to use on other body parts, and contact a doctor if experiencing chest pain, rapid heartbeat, or swelling in extremities. Additionally, it is recommended to consult a doctor before use if you have heart disease or if pregnant or breastfeeding. If accidentally swallowed, medical help should be sought immediately. The text also mentions the manufacturer's contact information and product details like pack size and supply duration.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.