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

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)

Amber glass bottle with a white child-resistant cap. The visible label includes usage directions and contact information for Sincerus Florida, LLC, the labeler of FINASTERIDE 0.1% / MINOXIDIL 7%. The label instructs external use and advises washing hands after application.*

FDA Label Image

X (4075 8 Front)

FINASTERIDE 0.1% / MINOXIDIL 7% solution in a brown bottle with a white screw cap. The label shows the NDC 72934-4075-8, compound drug designation, and Sincerus Florida, LLC branding in blue and orange. The net weight is 60 grams, and the product is made in the USA.*

FDA Label Image

G (4075 8 Middle)

FINASTERIDE 0.1% / MINOXIDIL 7% solution in a brown glass bottle with a white cap. The label lists active ingredients as Finasteride USP 0.1% and Minoxidil USP 7%, and inactive ingredients including Ethyl Alcohol USP 32.9%, Lactic Acid USP 5%, and Propylene Glycol USP 55%. The labeler is Sincerus Florida, LLC.*

* 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.