Niacinamide 4% / Tretinoin 0.05%
Product Images NDC 72934-1163

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 72934-1163). 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

F (1163 2 End)

Side label panel of NIACINAMIDE 4% / TRETINOIN 0.05% by Sincerus Florida, LLC. The label includes directions for use advising application as directed by a physician, topical use only, hand washing after use, and storing at controlled room temperature (20-25°C). Contact details for the manufacturer and FDA reporting information are also present.*

FDA Label Image

S (1163 2 Front)

NIACINAMIDE 4% / TRETINOIN 0.05% gel in a white plastic container. The label displays the NDC 72934-1163-2 and indicates a 30 gm quantity. The product is labeled as a compounded drug, made in the USA, and is from Sincerus Florida, LLC.*

FDA Label Image

D (1163 2 Middle)

Label of a prescription medication bottle for NIACINAMIDE 4% / TRETINOIN 0.05% gel by Sincerus Florida, LLC. The label lists active ingredients as Niacinamide USP 4% and Tretinoin USP 0.05%, with inactive ingredients including a gel base. The label includes batch and manufacturing dates as well as a lot number.*

* 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.