Minoxidil 5% / Progesterone 0.1% / Tretinoin 0.025%
Product Images NDC 72934-4146

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 5% / Progesterone 0.1% / Tretinoin 0.025% (NDC 72934-4146). 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

Fs (8 End)

Fs (8 End)
MINOXIDIL 5% / PROGESTERONE 0.1% / TRETINOIN 0.025% in a small amber glass bottle with a white screw cap. The label includes directions for use and contact information for Sincerus Florida, LLC, the labeler. The bottle is intended for topical application and external use only.*
FDA Label Image

Sf (4146 8 Front)

Sf (4146 8 Front)
This is a brown glass bottle with a white cap bearing a label for MINOXIDIL 5%, PROGESTERONE 0.1%, and TRETINOIN 0.025% solution by Sincerus Florida, LLC. The label includes the NDC 72934-4146 and indicates a 60gm compounded drug made in the USA.*
FDA Label Image

Qwe (4146 8 Middle)

Qwe (4146 8 Middle)
Brown glass bottle with a white child-resistant cap labeled for MINOXIDIL 5% / PROGESTERONE 0.1% / TRETINOIN 0.025% solution. The label lists active ingredients Minoxidil USP 5%, Progesterone USP 0.1%, and Tretinoin USP 0.025%, with inactive ingredients including Butylated HydroxyToluene NF, Ethyl Alcohol USP, and Propylene Glycol USP. 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.