Mupirocin Cream
Product Images NDC 69238-2029

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mupirocin (NDC 69238-2029). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny Llc, 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

Structural Formula (Mupirocin Cream Usp 2 Percent 1)

Structural Formula (Mupirocin Cream Usp 2 Percent 1)
Chemical structure of mupirocin, depicting its molecular configuration including calcium and water components as shown in the image.*
FDA Label Image

15 G Tube (Mupirocin Cream Usp 2 Percent 2)

15 G Tube (Mupirocin Cream Usp 2 Percent 2)
Label for Mupirocin Cream USP, 2%, topical cream in a 15 g package. The label shows the active ingredient strength (2%) and usage route (topical). It is labeled for prescription use only and distributed by Amneal Pharmaceuticals LLC. Storage instructions and dosage information are partially visible. A barcode and NDC number 69238-2029 are included.*
FDA Label Image

15 G Carton (Mupirocin Cream Usp 2 Percent 3)

15 G Carton (Mupirocin Cream Usp 2 Percent 3)
Mupirocin Cream USP, 2%, topical cream packaged in a 15 g tube. The label shows the product is distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. It includes directions for use, storage instructions, and a barcode. The label features the Amneal logo and indicates the product is prescription-only.*

* 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.