Calcipotriene 0.005% / Niacinamide 4%
Product Images NDC 72934-2033

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 Calcipotriene 0.005% / Niacinamide 4% (NDC 72934-2033). 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

Qd (2 End)

Qd (2 End)
Side view of a white cylindrical container label for CALCIPOTRIENE 0.005% / NIACINAMIDE 4% by Sincerus Florida, LLC. The label includes directions for use and manufacturer contact information with a small QR code at the bottom. The label advises storage at controlled room temperature (20-25°C).*
FDA Label Image

C (2033 2 Front)

C (2033 2 Front)
CALCIPOTRIENE 0.005% / NIACINAMIDE 4% cream in a 30 gram white container with a label showing the NDC 72934-2033-2. The label also features the Sincerus Florida, LLC logo and states that this is a compounded drug made in the USA.*
FDA Label Image

Sd (2033 2 Middle)

Sd (2033 2 Middle)
Side view of a white cylindrical container label for CALCIPOTRIENE 0.005% / NIACINAMIDE 4% cream, showing partial information including active ingredients (Calcipotriene Anhydrous USP 0.005% and Niacinamide USP 4%), inactive ingredient (Suspensisse Cream 95.995%), prescription status (Rx only), and lot and manufacturing dates. The label also shows the labeler name 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.