Minoxidil Topical Solution
Product Images NDC 59640-000

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Minoxidil Topical (NDC 59640-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H E B, 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

Graphic1 (Image 01)

An illustration showing four top-view images of a person's scalp indicating hair coverage. The first three images depict varying progression of hair density, while the fourth image shows a scalp with a large hair thinning or bald area marked with a circle and a diagonal line crossing it, indicating it is not recommended or a warning.*

FDA Label Image

Graphic2 (Image 02)

A stacked bar chart comparing hair regrowth in females after 8 months of treatment with placebo versus minoxidil. The y-axis shows percent of females, with bars indicating proportions achieving minimal and moderate regrowth. The minoxidil group shows higher percentages in both categories compared to placebo.*

FDA Label Image

Bottle-graphic1 (Image 03)

A black and white line drawing of a dropper bottle with a screw-on cap and a pipette inside. The bottle is cylindrical and appears designed for dispensing liquid topical solution.*

FDA Label Image

Minoxidil Topical Solution Image (Image 04)

Minoxidil topical solution USP, 2% by H E B is a topical solution for hair regrowth treatment for women. The packaging shows a 60 mL (2 FL OZ) bottle as a one month supply. The product is unscented and labeled as clinically proven to help regrow hair by reactivating hair follicles. The label compares the product to Women's Rogaine and provides usage instructions and warnings for safe application.*

* 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.