Fluocinolone Acetonide 0.01% / Niacinamide 4%
Product Images NDC 72934-2081

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% / Niacinamide 4% (NDC 72934-2081). 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

F (2 End)

F (2 End)
FLUOCINOLONE ACETONIDE 0.01% / NIACINAMIDE 4% in a white cylindrical container with a label showing directions for use, storage instructions, and contact information for Sincerus Florida LLC located in Pompano Beach, FL. The label mentions topical application and room temperature storage (20-25°C).*
FDA Label Image

D (2081 2 Front)

D (2081 2 Front)
Packaging label for FLUOCINOLONE ACETONIDE 0.01% / NIACINAMIDE 4% cream in a 30 gram container. The label includes the NDC 72934-2081-2 and indicates the product is a compounded drug made in the USA by Sincerus Florida LLC.*
FDA Label Image

D (2081 2 Middle)

D (2081 2 Middle)
A partial side view of the FLUOCINOLONE ACETONIDE 0.01% / NIACINAMIDE 4% cream container label showing the active ingredients section. It lists Fluocinolone Acetonide USP 0.01% and Niacinamide USP 4% as active ingredients, along with an inactive ingredients section mentioning the cream base. The label indicates Rx only status and includes lot and manufacturing 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.