Acid Reducer Tablet, Delayed Release
Product Images NDC 63941-006

2 FDA label images from Best Choice · 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 63941-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Best Choice, 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))
Acid Reducer Omeprazole delayed-release tablets 20 mg by Best Choice, in a 14-tablet package. The label highlights treatment of frequent heartburn, with directions and warnings included. The product is for oral use and carries information on usage, allergy warnings, and storage. Manufactured in India and distributed by Walu Merchandisers in Kansas City, KS.*
FDA Label Image

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

Package Label-principal Display Panel (20 mg Blister Carton Label)
Acid Reducer Omeprazole delayed-release tablets 20 mg by Best Choice. The label indicates a 14-tablet package designed for oral use, treating frequent heartburn with a 24-hour effect. The front displays active ingredient strength and treatment duration, with additional Drug Facts panels providing usage directions, warnings, and inactive ingredients. Manufactured in India and distributed by Best Choice, Kansas City.*

* 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.