Niacinamide 4% / Tretinoin 0.05%
Product Images NDC 72934-2163

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% / Tretinoin 0.05% (NDC 72934-2163). 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

Wd (2163 4 End)

Wd (2163 4 End)
A white cylindrical bottle of NIACINAMIDE 4% / TRETINOIN 0.05% topical product by Sincerus Florida, LLC. The bottle has a label containing directions for use and manufacturer contact information, including an address in Pompano Beach, FL, and a phone number. The label advises to apply topically as directed by a physician and to store at controlled room temperature.*
FDA Label Image

D (2163 4 Front)

D (2163 4 Front)
Packaging label on a white container for NIACINAMIDE 4% / TRETINOIN 0.05% cream, 120gm, by Sincerus Florida, LLC. The label includes the NDC number 72934-2163-4, the statement "This is a compounded drug," and "Made in USA." The label features the Sincerus Florida logo in teal and orange.*
FDA Label Image

Rf (2163 4 Middle)

Rf (2163 4 Middle)
NIACINAMIDE 4% / TRETINOIN 0.05% cream in a white cylindrical container. The label lists active ingredients as Niacinamide USP 4% and Tretinoin USP 0.05%, with inactive ingredients composing 95.95% of the suspension cream. The product is labeled as prescription only and manufactured by 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.