Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 21130-718

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Esomeprazole Magnesium (NDC 21130-718). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Better Living Brands, 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

718t_albertsons_ifc_14ct (718t Albertsons Ifc 14ct)

Packaging label for Esomeprazole Magnesium 20 mg delayed-release capsules by Better Living Brands, LLC. The label shows a 14-capsule bottle with a window on the carton. It highlights the product's use for treating frequent heartburn and includes Drug Facts, warnings, directions, inactive ingredients, and contact information. The label also compares the product to Nexium 24 HR and features a barcode and lot/expiration date fields.*

FDA Label Image

718t_albertsons_ifc_42ct (718t Albertsons Ifc 42ct)

Box packaging label for Esomeprazole Magnesium delayed-release capsules USP, 20 mg, by Better Living Brands LLC. The label states 42 capsules per bottle with a 14-day treatment supply. It features Drug Facts panels detailing active ingredients, uses, warnings, directions, and inactive ingredients. The label includes dosage form identification and a barcode.*

FDA Label Image

718t_albertsons_lbl_14ct (718t Albertsons Lbl 14ct)

Esomeprazole Magnesium 20 mg delayed-release capsules label from Signature Care, containing 14 capsules. The label includes drug facts such as active ingredient, purpose, usage instructions, warnings, and storage information. The labeler is Better Living Brands LLC, with a tamper-evident seal and recycling information displayed.*

* 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.