Mupirocin Ointment
Product Images NDC 50268-568

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mupirocin (NDC 50268-568). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

2% (Screen Shot 2019 06 11 At 1.24.34 Pm Copy)

The NDC code 50268-568-15 is associated with Mupirocin ointment, USP 2%, which is used for dermatologic use only and is not intended for ophthalmic use. The package includes 50 individual 1-gram tubes of ointment, each containing 20 mg of mupirocin in a polyethylene glycol ointment base. Patients are advised to apply a small amount of ointment three times daily and those who do not show a clinical response within 3 to 5 days should be re-evaluated. The medication should be stored at a temperature range of 20° to 25°C (68° to 77° F) and kept out of the reach of children. The manufacturer is AVKARE, Inc. and the package contains directions for puncturing the tube seal.*

FDA Label Image

Chemical Structure (Mupirocin 01)

* 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.