Metronidazole 1% / Mupirocin 2% /
Product Images NDC 72934-5151

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 Metronidazole 1% / Mupirocin 2% / (NDC 72934-5151). 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.

Product Images & Figures Index

FDA Label Image

E (2 End)

E (2 End)
Side view of a white cylindrical container with a label showing directions for use and manufacturer contact information. The product is METRONIDAZOLE 1% / MUPIROCIN 2%, labeled by Sincerus Florida, LLC. The label includes instructions for topical application and storage conditions, along with a QR code and contact phone numbers.*
FDA Label Image

S (5151 2 Front)

S (5151 2 Front)
Packaging label of METRONIDAZOLE 1% and MUPIROCIN 2% ointment in a 30 gram container. The label displays the NDC number 72934-5151-2 and indicates the product is a compounded drug made in the USA. The labeler is Sincerus Florida, LLC, with a logo featuring the words 'Sincerus' and 'Florida' on turquoise and orange backgrounds respectively.*
FDA Label Image

S (5151 2 Middle)

S (5151 2 Middle)
Label on a white container for METRONIDAZOLE 1% / MUPIROCIN 2% topical medication by Sincerus Florida, LLC. The label lists active ingredients as Metronidazole USP 1% and Mupirocin USP 2%, with inactive ingredients Aloe Vera 0.2% and Petrolatum 96.8%. It also includes manufacturing (01/01/1970) and expiration dates and 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.