Omeprazole Tablet, Delayed Release
Product Images NDC 56062-401

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 56062-401). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Publix Super Markets Inc, 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 Image 1 (Image 01)

Omeprazole Image 1 (Image 01)
Packaging label for omeprazole delayed release tablets 20 mg by Publix Super Markets Inc. The label indicates 42 wildberry mint coated tablets designed for acid reduction and frequent heartburn treatment. It features dosage instructions, safety warnings, and a comparison reference to Prilosec OTC®.*
FDA Label Image

Omeprazole Image 2 (Image 02)

Omeprazole Image 2 (Image 02)
Drug Facts panel for omeprazole 20 mg delayed-release oral tablets by Publix Super Markets Inc. Includes active ingredient, uses, warnings about allergies and symptoms, directions for adults 18 and older, 14-day treatment course details, repeated courses instructions, inactive ingredients list, storage information, and contact details for the distributor.*

* 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.