Acid Reducer Tablet, Delayed Release
Product Images NDC 58602-729

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Acid Reducer (NDC 58602-729). 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

Omeprazole Fig1

Acid Reducer Omeprazole Delayed-Release Tablets 20 mg label by Aurohealth LLC. The label includes the brand and generic name, strength, and quantity of 14 tablets. It displays directions, warnings, tamper evidence information, and tips for managing heartburn. The label is primarily purple with white text and outlines usage instructions and safety precautions for the oral delayed-release tablets.*

FDA Label Image

Omeprazole Fig2

Acid Reducer Omeprazole Delayed-Release Tablets 20 mg oral tablet packaging label by Aurohealth LLC. The purple carton contains 14 tablets designed for a 14-day treatment course, treating frequent heartburn for 24 hours. The label lists active ingredient omeprazole magnesium USP equivalent to 20.6 mg omeprazole and includes warnings, directions, inactive ingredients, storage information, and a barcode. Manufactured in India, NDC 58602-729-05.*

FDA Label Image

Omeprazole Fig3

The label for Acid Reducer Omeprazole Delayed-Release Tablets 20 mg shows a purple packaging with white and yellow text. It states the product is an acid reducer treating frequent heartburn for 24 hours. The label includes dosage instructions for a 14-day treatment course and highlights the active ingredient Omeprazole delayed-release tablet 20 mg. The labeler is Aurohealth LLC.*

FDA Label Image

Omeprazole Fig4

Acid Reducer Omeprazole Delayed-Release Tablets 20 mg oral tablet packaging label by Aurohealth LLC. The label features dosing information for a 14-tablet supply, with directions, warnings, and tips for managing heartburn. The design highlights the 24-hour symptom relief and includes the National Drug Code (NDC) 58602-729-01.*

* 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.