Esomeprazole Magnesium Tablet, Delayed Release
Product Images NDC 58602-840

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 58602-840). 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 Tablets))

Drug facts and warnings panel for Esomeprazole Magnesium delayed-release tablets 20 mg by Aurohealth LLC. It includes active ingredient details, usage instructions, allergies, warnings about severe skin reactions, heartburn treatment directions, caution for use in pregnancy or breastfeeding, overdose advice, and storage conditions. The label emphasizes a 14-day course and frequent heartburn treatment guidelines.*

FDA Label Image

Package Label-principal Display Panel (20 mg (14 Tablets))

Esomeprazole Magnesium Delayed-Release Tablets 20 mg by Aurohealth LLC. The packaging displays a white bottle with label and a color carton predominantly in pink, yellow, and white. It is indicated as an acid reducer for treating frequent heartburn, with a 14-tablet count for a 14-day course of treatment. The label includes drug facts, warnings, directions, active ingredients, and company contact information. The product NDC is 58602-840.*

* 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.