Mupirocin
Product Images NDC 81033-020

5 FDA label images from Kesin Pharma Corporation · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Mupirocin (NDC 81033-020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kesin Pharma Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of mupirocin, showing its detailed molecular arrangement with multiple rings, hydroxyl groups, methyl groups, and a carboxyl side chain, consistent with mupirocin's known chemical formula.*
FDA Label Image
Kesin Pharma Logo (Kesin Logo)
FDA Label Image
Kesin Pharma Logo (Kesin Logo)
FDA Label Image

Carton Of 50 (Mupoint Carton 1g 50 05212025 Image)

Carton Of 50 (Mupoint Carton 1g 50 05212025 Image)
Label for Mupirocin Ointment, USP 2%, a topical medication with 20 mg/g strength, packaged in 50 unit dose tubes of 1 gram each. Distributed by Kesin Pharma Corporation, this Rx-only ointment is for institutional use only and includes storage instructions of 68°F to 77°F (20°C to 25°C). The label also shows lot number, expiration date placeholders, and a barcode.*
FDA Label Image

Carton Of 100 (Mupoint Carton 1g 100 05212025 Image)

Carton Of 100 (Mupoint Carton 1g 100 05212025 Image)
Mupirocin Ointment USP 2% label for 1 gram unit dose tubes. The label indicates a package of 100 x 1g tubes, labeled for institutional use only, with storage instructions and manufacturer Kesin Pharma Corporation, Oldsmar, FL. The label includes barcode, QR code, and regulatory information.*

* 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.