Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1%
Product Images NDC 72934-4080

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 Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1% (NDC 72934-4080). 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

Zc (8 End)

Zc (8 End)
A brown glass bottle with a white ribbed screw cap, displaying a partial label with directions for use and contact information. The product is FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 7% / PROGESTERONE 0.1% by Sincerus Florida, LLC. The label includes storage instructions and a QR code.*
FDA Label Image

Zx (4080 8 Front)

Zx (4080 8 Front)
FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 7% / PROGESTERONE 0.1% solution in a brown glass bottle with a white cap. The label shows the NDC 72934-4080-8 and indicates the product is a compounded drug manufactured by Sincerus Florida, LLC, with a net content of 60 grams. The label also states it is made in the USA.*
FDA Label Image

Sd (4080 8 Middle)

Sd (4080 8 Middle)
FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 7% / PROGESTERONE 0.1% solution in a brown glass bottle with a white child-resistant cap. The label lists active ingredients Fluocinolone Acetonide USP 0.01%, Minoxidil USP 7%, and Progesterone USP 0.1%, along with inactive ingredients Ethyl Alcohol USP, Lactic Acid USP, and Propylene Glycol USP. The product is labeled Rx only and 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.