Niacinamide 4% / Tacrolimus 0.03%
Product Images NDC 72934-5158

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% / Tacrolimus 0.03% (NDC 72934-5158). 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

Sd (2 End)

Sd (2 End)
The image shows a white cylindrical container with a label providing directions for use and manufacturer contact information. The label instructs to apply the product topically as directed by a physician, for external use only, and to store at controlled room temperature (20-25°C). The label lists Sincerus Florida, LLC in Pompano Beach, FL, as the manufacturer, along with their contact phone number and FDA MedWatch reporting information.*
FDA Label Image

Fd (5158 2 Front)

Fd (5158 2 Front)
The image shows a white container labeled as NIACINAMIDE USP 4% and TACROLIMUS MONOHYDRATE USP 0.03% ointment in a 30 gm size. The label includes the NDC number 72934-5158-2 and features the logo of Sincerus Florida. It states that this is a compounded drug made in the USA.*
FDA Label Image

Dwd (5158 2 Middle)

Dwd (5158 2 Middle)
Side view of a white cylindrical container label showing active and inactive ingredients of NIACINAMIDE 4% / TACROLIMUS 0.03% ointment by Sincerus Florida, LLC. The label lists active ingredients as Niacinamide USP 4% and Tacrolimus Monohydrate USP 0.03%, with Petrolatum as the inactive ingredient at 95.97%. The label includes the lot number, manufacturing date, and a cautionary warning about long-term safety.*

* 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.