Mupirocin Ointment
Product Images NDC 51672-1312

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mupirocin (NDC 51672-1312). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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

Chemical Structure (Mupirocin 01)

FDA Label Image

Principal Display Panel (15 g Tube Carton)

Principal Display Panel (15 g Tube Carton)
Mupirocin is an ointment used for treating skin infections. This ointment contains 20 mg of Mupirocin per gram mixed in a polyethylene glycol ointment base of polyethylene glycol 400 and polyethylene glycol 3850. It is applied topically on the affected area three times a day. If the patient does not show improvement, re-evaluation is required. This medication is for dermatological purposes only, and not ophthalmic purposes. The prescription information is available in the packaging. The tube should be punctured on the tip instead of the cap. The medication should be stored at room temperature. The expiry date and batch number are located on the flap of the carton or crimp of the tube.*

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