Minoxidil 5% / Progesterone 0.1% / Tretinoin 0.025%
Product Images NDC 72934-4146

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Minoxidil 5% / Progesterone 0.1% / Tretinoin 0.025% (NDC 72934-4146). 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

Fs (8 End)

This is a set of directions for use of a product that should be applied externally only. Users should wash their hands after use, and the product should be stored at room temperature. The product is distributed by Sincerus Florida, LLC and should be used as directed. In case of adverse reactions, users should contact Sincerus Florida, LLC or the FDA. It is not available for resale.*

FDA Label Image

Sf (4146 8 Front)

This is a solution containing 2% Minoxidil USP and 0.1% Progesterone USP along with 0.025% Retinoin USP. The total quantity of the solution is 60gm.*

FDA Label Image

Qwe (4146 8 Middle)

This is a list of active and inactive ingredients found in a product. The active ingredients include Minoxidil, Progesterone, and Tretinoin. The inactive ingredients include Butylated Hydroxytoluene (BHT), Ethyl Alcohol, and Propylene Glycol.*

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