Fluocinolone Acetonide 0.01/ Niacinamide 4
Product Images NDC 72934-2084

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 72934-2084). 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

F (2 End)

F (2 End)
Side view of a white cylindrical container for FLUOCINOLONE ACETONIDE 0.01/ NIACINAMIDE 4. The label includes directions for use, storage instructions, and contact information for Sincerus Florida LLC in Pompano Beach, FL. The label also features a QR code and mentions that the product is for external use only and requires physician direction.*
FDA Label Image

X (2084 2 Front)

X (2084 2 Front)
Packaging label of FLUOCINOLONE ACETONIDE 0.025% and NIACINAMIDE 4% cream in a 30 gram container from Sincerus Florida LLC. The label includes the NDC 72934-2084-2 and indicates the product is a compounded drug made in the USA.*
FDA Label Image

C (2084 2 Middle)

C (2084 2 Middle)
FLUOCINOLONE ACETONIDE 0.01/ NIACINAMIDE 4 cream in a white cylindrical container with a label showing the active ingredients Fluocinolone Acetonide USP 0.025% and Niacinamide USP 4%. The label includes additional product details such as RX only, lot number, manufacturing and expiration dates, and the labeler 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.