Mupirocin Cream
Product Images NDC 68462-564
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This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Mupirocin (NDC 68462-564). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Glenmark Pharmaceuticals Inc., Usa, 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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This is a drug package label for Mupirocin Ointment USP, 2% manufactured by Glenmark Pharmaceuticals. It is a prescription medication used for dermatological purposes only. The ointment contains 20 mg of mupirocin per gram in an oil and water-based emulsion. The recommended dosage is to apply a small amount to the affected area three times a day for ten days. Patients who do not show a clinical response within 30-35 days should be re-evaluated. The product should be stored at a controlled room temperature of 20°C to 25°C (68°F to 77°F) and must not be frozen. The package should not be used if it has been punctured or if the drug is visible, and the cap should be used to puncture the seal.*
Tube 15g
Mupirocin cream is a topical antibiotic medication used to treat skin infections. It contains 20mg of mupirocin per gram and is applied to the affected area three times a day for 10 days. If no improvement is observed within 3-5 days, the patient should be re-evaluated. The cream should be stored between 20°C to 25°C and should not be frozen. It should not be used if the seal has been punctured or is not visible. Mupirocin cream is only recommended for dermatologic use. Please see accompanying prescribing information for more detail.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.