Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 60000-109

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 60000-109). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ahold U.s.a., 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))

Esomeprazole Magnesium 20 mg delayed-release capsules OTC packaging label from Ahold U.S.A., Inc. The blue and yellow carton includes directions for use, active ingredient and purpose, warnings, and a 14-capsule count indication. It states a 24-hour relief period and mentions a 14-day course of treatment for heartburn. The label also includes NDC 60000-109-15.*

FDA Label Image

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

CareOne Esomeprazole Magnesium Delayed-Release Capsules USP 20 mg carton label for oral use. The label displays the product as an acid reducer for frequent heartburn, containing 14 capsules per bottle. Manufactured by Ahold U.S.A., Inc, the packaging includes detailed drug facts, usage warnings, and a barcode on a blue background with yellow and white text.*

* 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.