Metronidazole 1% / Mupirocin 2%
Product Images NDC 72934-5143

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metronidazole 1% / Mupirocin 2% (NDC 72934-5143). 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

Ed (2 End)

A white cylindrical container label for METRONIDAZOLE 1% / MUPIROCIN 2% from Sincerus Florida, LLC. The label includes directions for use stating application is topical and for external use only, storage instructions at 20-25C, and contact information for reporting adverse reactions. A QR code is visible at the bottom.*

FDA Label Image

X (5143 2 Front)

White plastic container labeled with Metronidazole USP 1% and Mupirocin USP 2% ointment, 30 gm. The label includes the NDC number 72934-5143-2 and states it is a compounded drug made in the USA. The label also shows the Sincerus Florida logo with a teal and orange background.*

FDA Label Image

D (5143 2 Middle)

Side label of METRONIDAZOLE 1% / MUPIROCIN 2% topical ointment by Sincerus Florida, LLC displaying active ingredients Metronidazole USP 1% and Mupirocin USP 2%, along with inactive ingredients Aloe Vera 0.2%, Lavare 46.8%, and Petrolatum 50%. The label also shows 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.