Up And Up Lansoprazole Capsule, Delayed Release
Product Images NDC 11673-280

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Up And Up Lansoprazole (NDC 11673-280). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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

Lansoprazole-delayed-release-capsules-carton-image-1 (3t3d7uwc12 Image 1)

up and up lansoprazole delayed release capsules 15 mg packaging label shows a box with the proprietary and generic names, strength, and dosage form. It states acid reducer 24-hour and treats frequent heartburn. The labeler is Target Corporation. The box contains 42 capsules, noted as three 14-day courses of treatment, and displays an actual size image of one capsule, which is pink and green.*

FDA Label Image

Lansoprazole-delayed-release-capsules-carton-image-2 (3t3d7uwc12 Image 2)

Drug Facts panel for up and up lansoprazole 15 mg delayed-release oral capsules. The panel lists lansoprazole 15 mg as the active ingredient and provides information on use, warnings, directions for a 14-day treatment course, and repeated courses if needed. It includes tips for managing heartburn, storage instructions, inactive ingredients, and contact information for questions or comments. The labeler is Target Corporation.*

* 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.