Pirnuo Cream
Product Images NDC 68462-560

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pirnuo (NDC 68462-560). 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.

FDA Label Image

Structure (Structure)

FDA Label Image

Carton-pump (Carton Pump)

Carton-pump (Carton Pump)
PIRNUO Cream is a dermatologic medicine produced by Glenmark Pharmaceuticals. Each gram of the cream contains 20 mg (2% w/w) of mupirocin. The dosage is to apply a small amount of cream to the affected area three times daily for 10 days. PIRNUO is a prescription medicine, and patients not showing a clinical response within 3 to 5 days should be re-evaluated. For more information regarding the medicine, refer to the accompanying prescribing information. The cream must be stored at 20°C to 25°C (68°F to 77°F).*
FDA Label Image
FDA Label Image

Pump-bottle-label (Pump Bottle Label)

Pump-bottle-label (Pump Bottle Label)
This is a product description for Mupirocin Cream USP, 2%. Each gram contains 20 mg of mupirocin equivalent to 21.5 mg of mupirocin calcium, USP in an oil- and water-based emulsion. It is for dermatologic use only, and patients should apply a small amount three times daily for 10 days. Patients not showing a clinical response within 3 to 5 days should be re-evaluated. It is manufactured by Glenmark Pharmaceuticals Limited located in Colvale-Bardez, Goa India. This cream should be stored between 20°C to 25°C (68°F to 77°F).*

* 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.