Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 58602-707

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 58602-707). 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.

Product Images & Figures Index

FDA Label Image

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

Package Label-principal Display Panel (20 mg (14 Capsule Container Label))
Esomeprazole Magnesium 20 mg delayed-release capsules label by Aurohealth LLC. The label states the capsules are for acid reduction with a 24-hour effect and comes in a package of 14 capsules, designed for a one 14-day course of treatment. The label includes detailed warnings, usage instructions, active ingredients, inactive ingredients, and contact information for questions or comments.*
FDA Label Image

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

Package Label-principal Display Panel (20 mg (14 Capsule Container Carton))
Packaging label for Esomeprazole Magnesium delayed-release capsules USP, 20 mg by Aurohealth LLC. The label indicates the product is an acid reducer with 14 capsules per package, intended to treat frequent heartburn. It includes Drug Facts with active ingredient, usage instructions, warnings, storage information, and manufacturer details along with a barcode and lot/expiry fields. The design features purple, yellow, white, and orange colors.*

* 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.