Lidocaine 2% / Mupirocin 2%
Product Images NDC 72934-5139

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lidocaine 2% / Mupirocin 2% (NDC 72934-5139). 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

D (2 End)

Side view of a white cylindrical container for LIDOCAINE 2% / MUPIROCIN 2% by Sincerus Florida, LLC. The label includes directions for use, storage instructions, the manufacturer's address in Pompano Beach, FL, and contact information for reporting adverse reactions. There is also a QR code on the label.*

FDA Label Image

Z (5139 2 Front)

Packaging label of Lidocaine 2% / Mupirocin 2% ointment in a 30 gram container. The label shows the NDC 72934-5139-2 and indicates the product is a compounded drug made in the USA by Sincerus Florida, LLC. The label features the Sincerus Florida logo in teal and orange colors.*

FDA Label Image

D (5139 2 Middle)

Label on a white cylindrical container of LIDOCAINE 2% / MUPIROCIN 2% ointment from Sincerus Florida, LLC. The visible panel lists active ingredients as Lidocaine USP 2% and Mupirocin USP 2%, and inactive ingredients Aloe Vera 0.2% and Petrolatum 95.8%. The label includes lot number and manufacturing date details.*

* 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.