Niacinamide 4% / Triamcinolone Acetonide 0.1%
Product Images NDC 72934-2166

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 Niacinamide 4% / Triamcinolone Acetonide 0.1% (NDC 72934-2166). 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

S (2 End)

S (2 End)
Side view of a white container for NIACINAMIDE 4% / TRIAMCINOLONE ACETONIDE 0.1%, showing part of the label. Directions for use and manufacturer contact information for Sincerus Florida, LLC in Pompano Beach, FL are visible, along with a QR code. The label advises storage at controlled room temperature and external topical use only.*
FDA Label Image

D (2166 2 Front)

D (2166 2 Front)
NIACINAMIDE 4% / TRIAMCINOLONE ACETONIDE 0.1% cream in a 30gm white container. The label shows the NDC number 73294-2166-2 and indicates the product is a compounded drug. The labeler is Sincerus Florida, LLC, featuring a logo with teal and orange colors and text stating "SINCERUS FLORIDA." The product is made in the USA.*
FDA Label Image

E (2166 2 Middle)

E (2166 2 Middle)
Label of NIACINAMIDE 4% / TRIAMCINOLONE ACETONIDE 0.1% cream by Sincerus Florida, LLC showing active ingredients as Niacinamide USP 4% and Triamcinolone Acetonide USP 0.1%. Inactive ingredients listed as suspension cream 95.9%. The label includes manufacturing and expiration dates along with lot number information.*

* 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.