Minoxidil 7% / Tretinoin 0.025%
Product Images NDC 72934-4150

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% / Tretinoin 0.025% (NDC 72934-4150). 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.

Product Images & Figures Index

FDA Label Image

Ewe (8 End)

Ewe (8 End)
Transparent amber bottle with a white child-resistant cap, displaying a label with directions for use and contact information for Sincerus Florida, LLC. The drug is MINOXIDIL 7% / TRETINOIN 0.025%, labeled by Sincerus Florida, LLC, and includes instructions for topical application and storage conditions.*
FDA Label Image

Ff (4150 8 Front)

Ff (4150 8 Front)
Amber glass bottle with white child-resistant cap containing MINOXIDIL USP 7% and TRETINOIN USP 0.025% solution, 60 gm. The label displays NDC 72934-4150-8 and the Sincerus Florida logo, and states the product is a compounded drug made in the USA.*
FDA Label Image

Et (4150 8 Middle)

Et (4150 8 Middle)
MINOXIDIL 7% / TRETINOIN 0.025% solution in a small brown glass bottle with a white child-resistant cap. The label lists active ingredients Minoxidil USP 7% and Tretinoin USP 0.025%, along with inactive ingredients including Butylated Hydroxytoluene NF, Ethyl Alcohol USP, Lactic Acid USP, and Propylene Glycol USP. The label also indicates Rx Only status and is marked with a lot number and manufacturing date.*

* 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.