Acid Reducer Tablet, Delayed Release
Product Images NDC 58602-826

2 FDA label images from Aurohealth Llc · 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 Acid Reducer (NDC 58602-826). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth Llc, 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

Package Label-principal Display Panel (20 mg (14 Tablet Bottle))

Package Label-principal Display Panel (20 mg (14 Tablet Bottle))
Drug facts and directions text panel for Acid Reducer Omeprazole Delayed-Release Tablets 20 mg by Aurohealth LLC. The panel includes directions for use, warnings, allergy alert, storage information, inactive ingredients, and contact information. It instructs on a 14-day course of treatment for heartburn and includes precautions for use and potential side effects.*
FDA Label Image

Package Label-principal Display Panel (20 mg Container Carton Label)

Package Label-principal Display Panel (20 mg Container Carton Label)
Acid Reducer Omeprazole Delayed-Release Tablets 20 mg box packaging label by Aurohealth LLC. The label indicates a 14-tablet count for a 14-day course of treatment targeting frequent heartburn, providing relief for 24 hours. The main panel highlights the active ingredient and purpose, with detailed Drug Facts and directions on side panels including warnings, ingredients, and instructions for use. The packaging also includes a barcode and tamper-evident warning.*

* 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.