Omeprazole And Sodium Bicarbonate Capsule
Product Images NDC 58602-732

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 Omeprazole And Sodium Bicarbonate (NDC 58602-732). 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (20 mg/1100 mg (14 Capsules Container Label))

Package Label-principal Display Panel (20 mg/1100 mg (14 Capsules Container Label))
Packaging label for Omeprazole and Sodium Bicarbonate capsules by Aurohealth LLC. The label shows the product contains Omeprazole 20 mg and Sodium Bicarbonate 1100 mg per capsule. It includes safety warnings, directions for use, and contact information. The packaging indicates a 14-day course of treatment with 14 capsules per container, designed to treat frequent heartburn.*
FDA Label Image

Package Label-principal Display Panel (20 mg/1100 mg (42 Capsules Container Carton Label))

Package Label-principal Display Panel (20 mg/1100 mg (42 Capsules Container Carton Label))
Packaging label for Omeprazole and Sodium Bicarbonate Capsules, 20 mg/1100 mg, by Aurohealth LLC. The label states the product is clinically proven to treat frequent heartburn with 42 capsules per package. It highlights the combination of omeprazole acid reducer and sodium bicarbonate allowing absorption. Usage instructions, drug facts, warnings, and managing heartburn tips are included on the sides. Distributed by Aurohealth LLC in East Windsor, NJ.*

* 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.