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

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)

This text provides directions for use for an external product. It instructs to apply topically and recommends storing at a controlled room temperature. The product is manufactured and distributed by Sincerus Florida, LLC in Pompano Beach, FL. It also provides contact information for reporting adverse reactions to the manufacturer or FDA. The product is not for resale.*

FDA Label Image

Zx (4080 8 Front)

This appears to be a product code for a medication containing an active ingredient called "LUOCINOLONE Ac:ETONID" at a strength of "USP0.0105" or "1%". There is also a reference to NDC (National Drug Code) which is a unique identifier for medications in the United States. The remaining text is not readable and appears to be a error.*

FDA Label Image

Sd (4080 8 Middle)

This is a prescription medicine with fluocinolone acetonide USP and minoxidil USP as active ingredients. The manufacturing date is January 1, 1970, and the lot number is 031092ABCDEFGH@1. The medicine also contains Ethyl Alcohol USP, Lactic Acid USP, and Propylene Glycol USP as additional components.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.