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

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% / 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.

Product Images & Figures Index

FDA Label Image

Da (8 End)

Da (8 End)
MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025% in a brown glass bottle with a white cap. The visible label includes directions for use, manufacturer information for Sincerus Florida, LLC, and contact details for reporting adverse reactions and FDA MedWatch information. The bottle is intended for topical external use.*
FDA Label Image

Sf (4149 8 Front)

Sf (4149 8 Front)
Brown glass bottle with a white capped lid labeled as MINOXIDIL USP 7%, PROGESTERONE USP 0.1%, and TRETINOIN USP 0.025% solution, 60gm. The label includes the NDC 72934-4149 and displays the Sincerus Florida logo. It states the product is a compounded drug made in the USA.*
FDA Label Image

Sw (4149 8 Middle)

Sw (4149 8 Middle)
Bottle packaging label for MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025% solution by Sincerus Florida, LLC. The label lists active ingredients minoxidil USP 7%, progesterone USP 0.1%, and tretinoin USP 0.025%, alongside inactive ingredients. The product is marked Rx only with a lot number and manufacturing dates visible.*

* 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.