Product Images Betamethasone Diproprionate 0.05% / Minoxidil 7%

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 3 images provide visual information about the product associated with Betamethasone Diproprionate 0.05% / Minoxidil 7% NDC 72934-4025 by Sincerus Florida, Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

fh - 8 end

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.*

zc - 4025 8 front

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.*

ss - 4025 8 middle

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.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.