Up And Up Omeprazole Tablet, Delayed Release
Product Images NDC 11673-018

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Up And Up Omeprazole (NDC 11673-018). 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

Image 01

The packaging label for up and up omeprazole 20 mg delayed release tablets features a white and magenta color scheme. The front displays the product name, dosage form, and strength along with the active ingredient indication as an acid reducer for frequent heartburn. It shows the up and up logo, mentions 42 tablets (three 14-day courses), and includes an image of three white bottles with purple caps. The label highlights the wildberry mint coated tablets, actual tablet size, and 24-hour effectiveness. Safety and usage tips are in smaller text on top panels.*

FDA Label Image

Image 02

Drug Facts panel for up and up omeprazole 20 mg delayed release tablets. Provides active ingredient and purpose, usage instructions, warnings, directions for a 14-day treatment course, inactive ingredients, and storage information. Includes safety advice and contact number for questions, emphasizing proper use and precautions.*

* 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.