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.*

* 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.