Minoxidil Solution
Product Images NDC 56062-322

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Minoxidil (NDC 56062-322). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Publix Super Markets 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

Vertex (Image 01)

An illustration showing three top-down views of a human scalp, each highlighting the vertex area with a labeled white box and arrow pointing to the center of the scalp. The diagrams emphasize the vertex region, commonly targeted in hair treatment applications.*

FDA Label Image

Bottle (Image 02)

An illustration showing a dropper bottle with the dropper partially removed from the bottle. The bottle has a threaded neck and the dropper has a bulb top and a pipette tube. The image likely represents the dispensing mechanism of a topical solution.*

FDA Label Image

Minoxidil Carton Image 1 (Image 03)

Minoxidil topical solution USP 5% 60 mL (2 fl oz) bottle label for Extra Strength for Men by Publix Super Markets Inc. The label shows the product as unscented, a hair regrowth treatment with a white bottle and dropper image at actual size. It states key features, usage restrictions, and comparison to Men's Rogaine active ingredient.*

FDA Label Image

Minoxidil Carton Image 2 (Image 04)

Minoxidil 5% topical solution for men, 5 g/100 mL, by Publix Super Markets Inc. The carton features hair regrowth illustrations for vertex scalp application, usage directions, drug facts, warnings, and package contents including a 60 mL bottle with one child-resistant dropper applicator. The product is for external use, applied twice daily on the scalp's hair loss area.*

* 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.