011020 Niacinamide 4% / Tretinoin 0.05%
Product Images NDC 72934-1204

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for 011020 Niacinamide 4% / Tretinoin 0.05% (NDC 72934-1204). 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

S (2 End)

Label on a white cylindrical container for 011020 NIACINAMIDE 4% / TRETINOIN 0.05% by Sincerus Florida, LLC. The label includes directions for use advising application as directed by a physician, external use only, hand washing after use, and storage at controlled room temperature (20-25°C). Manufacturer contact information in Pompano Beach, FL, is provided, along with FDA MedWatch reporting instructions and a QR code.*

FDA Label Image

S (1204 2 Front)

Bottle label of 011020 Niacinamide 4% / Tretinoin 0.05% gel, 30gm, from Sincerus Florida, LLC. The label shows the NDC 72934-1204-2 and includes a disclaimer that it is a compounded drug made in the USA. The design features the Sincerus Florida logo in blue and orange colors.*

FDA Label Image

S (1204 2 Middle)

The image shows a white cylindrical container label for 011020 NIACINAMIDE 4% / TRETINOIN 0.05% gel produced by Sincerus Florida, LLC. The label includes the active ingredients Niacinamide USP (4%) and Tretinoin USP (0.05%) along with inactive ingredients listed as Suspensidisse Gel. The product is labeled as Rx only and comes in a 30g gel form.*

* 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.