Finasteride 0.1% / Minoxidil 7% / Tretinoin 0.025%
Product Images NDC 72934-4076

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Finasteride 0.1% / Minoxidil 7% / Tretinoin 0.025% (NDC 72934-4076). 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

F (8 End)

FINASTERIDE 0.1% / MINOXIDIL 7% / TRETINOIN 0.025% in a brown glass bottle with a white screw cap. The label shows directions for use and manufacturer details for Sincerus Florida, LLC, including storage instructions and contact information. The product is intended for topical use and office use only.*

FDA Label Image

C (4076 8 Front)

A brown glass bottle with a white screw cap labeled as FINASTERIDE 0.1% / MINOXIDIL 7% / TRETINOIN 0.025% solution, 60gm, by Sincerus Florida, LLC. The label includes the NDC 72934-4076-8 and states it is a compounded drug made in the USA.*

FDA Label Image

S (4076 8 Middle)

Brown glass bottle with white child-resistant cap containing FINASTERIDE 0.1% / MINOXIDIL 7% / TRETINOIN 0.025% solution. Label shows active ingredients with their concentrations and inactive ingredients. The label also includes lot number 0331085 and expiration date 01/01/1970, manufactured 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.