Acid Reducer Tablet, Delayed Release
Product Images NDC 57483-120

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 Acid Reducer (NDC 57483-120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Innovus Pharmaceuticals, 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))
Acid Reducer Omeprazole Delayed-Release Tablets 20 mg label with Omeprazole as the active ingredient. The label states it contains 14 tablets, each a 14-day course of treatment, produced by Innovus Pharmaceuticals, Inc. It provides directions, warnings, and usage information for managing heartburn and includes tamper-evident instructions. The label is primarily white with purple and pink design elements, and includes barcode and lot information.*
FDA Label Image

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

Ackage Label-principal Display Panel (20 mg Container Carton Label)
Acid Reducer Omeprazole Delayed-Release Tablets 20 mg packaging label by Innovus Pharmaceuticals, Inc. The carton contains 42 tablets in a triple pack of 3x14 count bottles. The label highlights heartburn relief, delayed-release formulation, and provides directions, warnings, inactive ingredients, and manufacturer details. It states the product is not manufactured or distributed by AstraZeneca Pharmaceuticals.*

* 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.