Mupirocin Ointment
Product Images NDC 0121-1076

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mupirocin (NDC 0121-1076). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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 Of Mupirocin (Mup Oint 1)

Chemical structure of Mupirocin showing its molecular configuration with multiple hydroxyl groups, an ester linkage, and a carboxylic acid side chain.*

FDA Label Image

1 G Tube (Mup Oint 2)

Mupirocin ointment USP 2% label showing 20 mg/g strength for topical use only. The label includes storage instructions to keep at 20 to 25 degrees Celsius, a warning to use externally, and indicates the labeler as PAI Holdings, LLC dba PAI Pharma. The NDC code 0121-1076 is visible along with a barcode.*

FDA Label Image

50 Count Carton (Mup Oint 3)

Flat carton packaging label for Mupirocin Ointment USP, 2%, topical ointment, with a net content of 50 units x 1 gram. The label includes instructions noting it is for dermatologic use only and not for ophthalmic use. Distributed by PAI Pharma, this product is intended for prescription use only and labeled with the NDC 0121-1076-50.*

FDA Label Image

100 Count Carton (Mup Oint 4)

Packaging label for Mupirocin Ointment USP, 2%, a topical ointment in unit dose form with 100 units of 1 gram each. The label shows it is for dermatologic use only, prescription use by PAI Holdings, LLC dba PAI Pharma. The product is distributed from Greenville, SC, and the label includes dosage and storage instructions along with the NDC code 0121-1076.*

* 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.