Image 1
Mupirocin Ointment
Product Images NDC 0093-1010
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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mupirocin (NDC 0093-1010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Teva Pharmaceuticals Usa, 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.
Image 2
Mupirocin ointment is a dermatologic medication used externally only. It should not be applied to the eyes. The suggested dosage is applying a small amount of the ointment three times a day to the affected area, and if no response is seen within 3 to 5 days, the patient should be reevaluated. Patients experiencing rash, itching, or swelling after use should contact their healthcare provider. Each gram of the ointment contains 20mg mupirocin in a polyethylene glycol NF base. NDC code for this medication is 0093-1010-42. The text also has some printing information related to Elvahart Pharmaceuticals USA, Inc. and a barcode.*
* 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.
