Finasteride 0.1% / Minoxidil 5%
Product Images NDC 72934-4074

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 Finasteride 0.1% / Minoxidil 5% (NDC 72934-4074). 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

Fv (8 End)

Fv (8 End)
Amber glass bottle with a white ribbed cap showing a partial label containing directions for use and contact information. The product is Finasteride 0.1% / Minoxidil 5% by Sincerus Florida, LLC. The label instructs applying topically for external use only and includes manufacturer contact details and storage instructions.*
FDA Label Image

Ut (4074 8 Front)

Ut (4074 8 Front)
Brown plastic bottle with white child-resistant cap containing FINASTERIDE 0.1% and MINOXIDIL 5% solution. The front label displays the product name, active ingredient strengths, and solution quantity of 60 grams. It is labeled as a compounded drug by Sincerus Florida, LLC, and includes the NDC number 72934-4074-8.*
FDA Label Image

;klm (4074 8 Middle)

;klm (4074 8 Middle)
FINASTERIDE 0.1% / MINOXIDIL 5% solution in a brown glass bottle with a white ribbed cap. The label shows active ingredients Finasteride USP 0.1% and Minoxidil USP 5%, along with inactive ingredients Ethyl Alcohol USP 44.9% and Propylene Glycol USP 50%. The label also indicates it is an Rx only product with lot and date information partially visible. Manufactured and labeled 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.