Betamethasone Diproprionate 0.05% / Minoxidil 7%
Product Images NDC 72934-4025

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Betamethasone Diproprionate 0.05% / Minoxidil 7% (NDC 72934-4025). 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

Fh (8 End)

This is a set of directions for use of an external product. The user is advised to apply it topically and to wash their hands after use. The product should be stored at a controlled room temperature. The contact information for the manufacturer, Sincerus Florida, LLC, is provided for reporting any adverse reactions. It is mentioned that the product is not for resale and is meant for office use only.*

FDA Label Image

Zc (4025 8 Front)

Betamethasone Dipropionate USP 0.05% and Minoxidil USP 7% are the active ingredients of this solution. The total weight of the solution is 60gm. No other information is available due to the text being incomplete.*

FDA Label Image

Ss (4025 8 Middle)

This is a description of a prescription label. The medication is called "Rx onty" and the lot number is "O3 0B0ABCODEFGH@N." The expiration date (BUD) is January 1st, 1970. The active ingredients are Betamethasone Dipropionate USP and Minoxidil USP. Ethyl Alcohol USP is also listed as an inactive ingredient.*

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