Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 70000-0731

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 70000-0731). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leader/ Cardinal Health 110, Inc., 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))

This text contains information about a 24-hour esomeprazole magnesium delayed-release capsule used for treating frequent heartburn. It provides directions for usage, warnings, possible allergic reactions, and important considerations before use. The product is meant for adults over 18 years of age and should be taken once a day for 14 days or as directed by a doctor. It is also advised not to exceed the recommended dosage and to seek medical help in case of overdose. Additionally, the text lists the inactive ingredients and provides a contact number for questions or comments regarding the product.*

FDA Label Image

Package Label-principal Display Panel (20 mg (28 Capsule Container Carton))

This is information about Esomeprazole Magnesium Delayed-Release Capsules USP, a type of acid reducer used to treat frequent heartburn. It is a generic version of Nexium 24HR. It may take 1 to 4 days to reach full effectiveness. The packaging includes important details such as lot number and expiration date for quality control and safety.*

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