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

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 58602-822). 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))

Package Label-principal Display Panel (20 mg (14 Capsule Bottle))
This is a medical description for an Acid Reducer product. The product contains the active ingredient Vlmma which is Esunegrazk 20 mg. It can treat Frequent Heartburn. The label warns against using the product in case of difficulty or pain while swallowing food, vomiting blood, or bloody or black stools. It contains instructions such as not to take more than 14 Gy and not to take the capsule for more than 14 days. The description also includes contact information for customer support.*
FDA Label Image

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

Package Label-principal Display Panel (20 mg Container Carton Label)
This is a product description and drug facts for Esomeprazole Magnesium Delayed-Release Capsules, USP 20 mg, used for frequent heartburn treatment. The text includes active and inactive ingredients, uses, warnings, and directions for use. It also includes contact information for questions and concerns.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.