Finasteride 0.1% / Minoxidil 7%
Product Images NDC 72934-4075

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Finasteride 0.1% / Minoxidil 7% (NDC 72934-4075). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, Llc, 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

C (4075 8 End)

FDA Label Image

X (4075 8 Front)

X (4075 8 Front)
This is a medication label that includes the National Drug Code (NDC) and the ingredients of the medication. It contains Finasteride USP at 0.1% concentration and Minoxidil USP at 7% concentration. The meaning for "0 N Q" is not available.*
FDA Label Image

G (4075 8 Middle)

G (4075 8 Middle)
Active ingredients are Minoxidil USP and Propylene USP.*

* 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.