Omeprazole Magnesium Capsule, Delayed Release
Product Images NDC 21130-398

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Omeprazole Magnesium (NDC 21130-398). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Albertsons Companies, 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

Bottle_label_14_ct (Bottle)

Omeprazole delayed-release capsules 20 mg by Albertsons Companies. The label states the product is an acid reducer treating frequent heartburn with a 14-day course of treatment, available in a 14-capsule safety-sealed package. Additional information includes usage instructions, warnings, and distributor contact details.*

FDA Label Image

Carton_label_14_ct (Carton)

Omeprazole Magnesium 20 mg delayed-release capsules packaging label from Albertsons Companies. The label includes product usage as an acid reducer, a safety-sealed 14-capsule count, and overdose, warnings, and directions information. It also features barcode, tamper-evident instructions, inactive ingredients, and customer service contact. The label states the product is distributed by Better Living Brands LLC and is made in India.*

* 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.