Fluocinolone Acetonide 0.01% / Minoxidil 5% / Tretinoin 0.025%
Product Images NDC 72934-4079

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 5% / Tretinoin 0.025% (NDC 72934-4079). 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

Sd (8 End)

FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 5% / TRETINOIN 0.025% in a small brown glass bottle with a white screw cap. The visible label side shows partial directions for use and contact details for Sincerus Florida, LLC, the labeler. The bottle appears to be for topical solution application.*

FDA Label Image

Sf (4079 8 Front)

A brown glass bottle with a white screw cap labeled FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 5% / TRETINOIN 0.025% solution 60gm. The label includes the NDC 72934-4079-8 and the logo for Sincerus Florida, LLC. The label states this is a compounded drug made in the USA.*

FDA Label Image

Fds (4079 8 Middle)

FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 5% / TRETINOIN 0.025% in a brown glass bottle with a white cap. The label lists active ingredients including Fluocinolone Acetonide USP 0.01%, Minoxidil USP 5%, and Tretinoin USP 0.025%. It also shows inactive ingredients such as Butylated Hydroxytoluene NF, Ethyl Alcohol USP, and Propylene Glycol USP. The labeler is Sincerus Florida, LLC, with a product NDC of 72934-4079.*

* 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.