Mupirocin Ointment
Product Images NDC 50268-568

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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.

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FDA Label Image

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

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)

Chemical Structure (Mupirocin 01)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.