Minoxidil 7% / Niacinamide 4%
Product Images NDC 72934-4147

3 FDA label images from Sincerus Florida, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Minoxidil 7% / Niacinamide 4% (NDC 72934-4147). 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

Ed (8 End)

Ed (8 End)
MINOXIDIL 7% / NIACINAMIDE 4% transparent brown glass bottle with a white ribbed screw cap. The visible label contains directions for use and contact information for Sincerus Florida, LLC, the labeler. The bottle appears intended for external topical use only, with usage instructions and storage conditions detailed.*
FDA Label Image

Sf (4147 8 Front)

Sf (4147 8 Front)
Amber bottle with a black screw cap labeled MINOXIDIL USP 7% and NIACINAMIDE USP 4% solution, 60gm. The label also shows NDC 72934-4147-8 and the Sincerus Florida logo with teal and orange colors. It states the product is a compounded drug made in the USA.*
FDA Label Image

Ca (4147 8 Middle)

Ca (4147 8 Middle)
Brown glass bottle with a black ribbed screw cap, partially showing a white label listing active and inactive ingredients including Minoxidil USP and Niacinamide USP. The label also includes the lot number, manufacturing date, and the product is identified as MINOXIDIL 7% / NIACINAMIDE 4% by Sincerus Florida, LLC.*

* 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.