Minoxidil 7% / Progesterone 0.1% / Tretinoin 0.025%
Product Images NDC 72934-4149

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Minoxidil 7% / Progesterone 0.1% / Tretinoin 0.025% (NDC 72934-4149). 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

Da (8 End)

This text provides directions for the use of a certain product. It is meant for external use only and should be applied topically. After use, it is advised to wash hands thoroughly. The product should be stored at a controlled room temperature, ranging from 20-25 degrees Celsius. For reporting adverse reactions, the contact information of the manufacturer and the FDA is provided. This text is not intended for resale and is for office use only.*

FDA Label Image

Sf (4149 8 Front)

This is a medication solution containing 28% Minoxidil USP, 5% Progesterone USP 0.1%, and Tretinoin USP 0.025% in a 60gm container. It could be used for hair growth or other medical conditions.*

FDA Label Image

Sw (4149 8 Middle)

This appears to be a description of a prescription medication, including the lot number, expiration date, and active and inactive ingredients. However, the text contains several errors, such as distorted characters and incomplete words, resulting from poor quality. Thus, the description is difficult to understand and may not be reliable.*

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