Careone Omeprazole Tablet, Delayed Release
Product Images NDC 41520-802

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Careone Omeprazole (NDC 41520-802). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Sales Company, 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

Careone-omeprazole-wildberry-mint-carton-image-1.jpg (Careone Omeprazole Wildberry Mint Carton Image 1)

CareOne Omeprazole 20 mg delayed release tablets packaging label. The label indicates 42 tablets, in three 14-day courses of treatment, wildberry mint coated tablets. It highlights use as an acid reducer for frequent heartburn, a 24-hour effect, and directions to swallow without chewing. The labeler is American Sales Company.*

FDA Label Image

Careone-omeprazole-wildberry-mint-carton-image-2.jpg (Careone Omeprazole Wildberry Mint Carton Image 2)

Drug Facts panel for careone omeprazole 20 mg delayed-release oral tablets by American Sales Company. The panel includes active ingredient, purpose as acid reducer, usage instructions, warnings, directions for 14-day treatment, and other information such as storage and inactive ingredients. Contact information and distributor details are also present.*

* 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.