Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 58602-846

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 58602-846). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth 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

Package Label-principal Display Panel (20 mg (14 Capsule Container Label))

The image shows the packaging label for Esomeprazole Magnesium Delayed-Release Capsules USP 20 mg by Aurohealth LLC. It includes the product name, strength (20 mg), dosage form (delayed-release capsules), quantity (14 capsules), and usage as an acid reducer for frequent heartburn treatment. Additional labeling details include warnings, active ingredient information, usage instructions, and manufacturer information printed on multiple label sections (Top Ply and Bottom Ply).*

FDA Label Image

Package Label-principal Display Panel (20 mg (42 Capsule Container Carton))

Packaging label for Esomeprazole Magnesium Delayed-Release Capsules USP 20 mg, an oral acid reducer by Aurohealth LLC. The label indicates 42 capsules total, divided into 3 bottles of 14 capsules each, designed for a 24-hour dosing period. It includes drug facts, directions, warnings, and a barcode, with a yellow and purple color scheme.*

* 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.