Mupirocin Cream
Product Images NDC 62332-624

3 FDA label images from Alembic Pharmaceuticals Inc. · 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 62332-624). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals 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.

FDA Label Image

Image (Fa444224 A0df 47cc A925 A53dcdc26dc5 01)

Image (Fa444224 A0df 47cc A925 A53dcdc26dc5 01)
Chemical structure diagram of mupirocin calcium salt, showing molecular components including calcium ion (Ca2+). The illustration depicts the arrangement of atoms and bonds characteristic of mupirocin's active ingredient.*
FDA Label Image

15 G Tube (Fa444224 A0df 47cc A925 A53dcdc26dc5 02)

15 G Tube (Fa444224 A0df 47cc A925 A53dcdc26dc5 02)
Label for Mupirocin Cream USP 2% topical cream, 15 grams, by Alembic Pharmaceuticals Inc. The label states each gram contains 20 mg mupirocin equivalent to 21.5 mg mupirocin calcium in a mineral oil cream base. It includes storage instructions, lot number and expiration date location, and a barcode with the product NDC 62332-624-15.*
FDA Label Image

15 G Carton (Fa444224 A0df 47cc A925 A53dcdc26dc5 03)

15 G Carton (Fa444224 A0df 47cc A925 A53dcdc26dc5 03)
Mupirocin Cream USP 2%, 15 grams tube packaging label for topical use. The label displays the brand Alembic, NDC 62332-624-15, and states the product is Rx only. Instructions for use, storage, and sealing are included. Manufactured by Aleor Dermaceuticals Ltd, India, for Alembic Pharmaceuticals, Inc., USA.*

* 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.