Betamethasone Dipropionate 0.05% / Minoxidil 5%
Product Images NDC 72934-4023

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Betamethasone Dipropionate 0.05% / Minoxidil 5% (NDC 72934-4023). 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

E (4023 8 End)

Sincerus Florida, LLC is a company located in Pompano Beach, EL 33069, with a telephone number of (800) 604-5032. The rest of the text is not-readable.*

FDA Label Image

X (4023 8 Front)

This appears to be a label for a medication that includes information on the product name, strength, and quantity. The medication is likely a solution that contains betamethasone and gentamicin, with a concentration of betamethasone propionate USP 0.05% and gentamicin sulfate USP 5%. However, some characters are illegible or appear to be errors in the process, so the information may not be fully accurate.*

FDA Label Image

X (4023 8 Middle)

This is a medication description. The active ingredients are Betamethasone Dipropionate USP and Minoxidil USP, while the inactive ingredients are Ethyl Alcohol USP and Propylene Glycol USP. Unfortunately, there is an extra "-" at the end which may be a mistake.*

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