Minoxidil 7% / Progesterone 0.1%
Product Images NDC 72934-4748

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% (NDC 72934-4748). 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

C (4748 8 End)

C (4748 8 End)
MINOXIDIL 7% / PROGESTERONE 0.1% in a dark amber glass bottle with a white child-resistant cap. The label includes directions for use, manufacturer information (Sincerus Florida, LLC), and contact details for reporting adverse reactions. The product is for topical, external use and should be stored at controlled room temperature.*
FDA Label Image

D (4748 8 Front)

D (4748 8 Front)
MINOXIDIL 7% / PROGESTERONE 0.1% solution in a 60gm amber bottle with a white child-resistant cap. The label includes the NDC number 72934-4748-8 and identifies the product as compounded by Sincerus Florida, LLC, made in the USA. The label also states that this is a compounded drug.*
FDA Label Image

Z (4748 8 Middle)

Z (4748 8 Middle)
Bottle label for MINOXIDIL 7% / PROGESTERONE 0.1% solution by Sincerus Florida, LLC. The label lists active ingredients Minoxidil USP 7% and Progesterone USP 0.1%, and inactive ingredients Ethyl Alcohol USP 32.9%, Lactic Acid USP 5%, and Propylene Glycol USP 55%. The label also shows Rx only and includes manufacturing and expiration dates.*

* 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.