Niacinamide 4% / Tretinoin 0.025%
Product Images NDC 72934-2162

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 0.025% (NDC 72934-2162). 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

C (2162 2 End)

C (2162 2 End)
The image shows a white cylindrical container with a detailed label. The label includes directions for use advising application as directed by a physician, external use only, and hand washing after use. It lists Sincerus Florida, LLC as the labeler, including contact information at 3265 W McNab Rd, Pompano Beach, FL 33069 with a phone number. There is also a QR code on the label. The product corresponds to NIACINAMIDE 4% / TRETINOIN 0.025% by Sincerus Florida, LLC.*
FDA Label Image

Abc (2162 2 Frront)

Abc (2162 2 Frront)
NIACINAMIDE 4% / TRETINOIN 0.025% cream in a 30gm white container with a label indicating it is a compounded drug made in the USA. The label includes the NDC 72934-2162-2 and the brander name Sincerus Florida, LLC with a teal and orange logo.*
FDA Label Image

S (2162 2 Middle)

S (2162 2 Middle)
Side label of NIACINAMIDE 4% / TRETINOIN 0.025% cream by Sincerus Florida, LLC, listing the active ingredients as Niacinamide USP 4% and Tretinoin USP 0.025%, with inactive ingredients comprising 95.975% of the composition. The label also shows the product is Rx only, with a lot number and manufacturing and expiration dates.*

* 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.