Omeprazole Tablet, Delayed Release
Product Images NDC 69168-476

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 69168-476). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allegiant Health, 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

Omeprazole Label (476 Omeprazole Delayed Release Tablet 1)

Omeprazole Label (476   Omeprazole Delayed Release Tablet 1)
Label set for Omeprazole 20 mg delayed-release tablets by Allegiant Health. The primary label shows the product name, strength, dosage form, and 14 tablets count with usage details for frequent heartburn. Additional label layers include ingredient and purpose information, batch details with manufacturing info, and usage instructions with safety sealing warnings.*
FDA Label Image

Omeprazole Carton (476 Omeprazole Delayed Release Tablet 2)

Omeprazole Carton (476   Omeprazole Delayed Release Tablet 2)
The packaging label for Omeprazole delayed-release tablets 20 mg by Allegiant Health displays the brand name prominently with 'ACID REDUCER' and highlights a 24-hour effect for frequent heartburn treatment occurring 2 or more days a week. The box indicates a 14-tablet count for a one 14-day course of treatment and includes detailed Drug Facts panels on the sides with active ingredients, usage, warnings, directions, and inactive ingredients information. The label also shows the Allegiant Health logo and notes that the product is not manufactured or distributed by Procter & Gamble, distributor of Prilosec OTC.*

* 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.