Acid Reducer Tablet, Delayed Release
Product Images NDC 49035-983

2 FDA label images from Wal-mart Stores, Inc. · 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 49035-983). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wal-mart Stores, 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

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

Package Label-principal Display Panel (20 mg (14 Tablet Bottle))
The image displays a packaging label for equate Omeprazole Delayed-Release Tablets 20 mg, branded as Acid Reducer by Wal-Mart Stores, Inc. The label highlights the product as a 14-tablet supply, designed to treat frequent heartburn for 24 hours with a 14-day course of treatment. Additional label details include tamper-evident warnings, management tips for heartburn, active ingredient and usage instructions, warnings, and storage information. The label states distribution by Wal-Mart in Bentonville, AR, with the product made in India.*
FDA Label Image

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

Package Label-principal Display Panel (20 mg Container Carton Label)
Packaging label for Equate Omeprazole Delayed-Release Tablets 20 mg, Acid Reducer by Wal-Mart Stores, Inc. The label indicates a 3-pack with 42 tablets total, designed for three 14-day courses of treatment to manage frequent heartburn. The box features dosage information, comparisons to Prilosec OTC active ingredient, directions, warnings, and tamper-evident information. The product is distributed by Walmart Inc., Bentonville, AR.*

* 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.