Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 58602-822

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 58602-822). 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 Bottle))

Label for Esomeprazole Magnesium 20 mg delayed-release capsules by Aurohealth LLC. The label indicates the product is an acid reducer for treating frequent heartburn with a 14-capsule count for a 14-day course, with instructions and warnings on the reverse side. It also includes active and inactive ingredient details and usage directions.*

FDA Label Image

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

The packaging label of Esomeprazole Magnesium Delayed-Release Capsules USP 20 mg by Aurohealth LLC features a yellow and purple design with branding from PrimaryHealth. The front indicates it treats frequent heartburn and contains 14 capsules for a 14-day course. Active ingredient is esomeprazole magnesium 20 mg per capsule. The label includes Drug Facts, Directions, Warnings, and inactive ingredients, along with a barcode and storage instructions.*

* 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.