Acid Reducer Tablet, Delayed Release
Product Images NDC 58602-850

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 Acid Reducer (NDC 58602-850). 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 (14 Tablet Bottle))

Package Label-principal Display Panel (20 mg (14 Tablet Bottle))
The image shows a multi-page packaging label for Acid Reducer Omeprazole Delayed-Release Tablets 20 mg by Aurohealth LLC. The top ply displays the product name, dosage form, strength, and quantity (14 tablets). The back of the top ply includes active ingredient details, usage instructions, warnings, and distributor information. The bottom ply contains detailed directions for use, precautions, and storage instructions. The label mentions the product is for oral use and treats frequent heartburn with a 24-hour effect.*
FDA Label Image

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

Package Label-principal Display Panel (20 mg Container Carton Label)
The packaging label for Aurohealth LLC's Acid Reducer Omeprazole Delayed-Release Tablets 20 mg features a purple and teal design with a heart graphic. It indicates 42 tablets per package and highlights that it treats frequent heartburn with three 14-day treatment courses. The label includes the NDC 58602-850-62 and states the product is made in India. "No Coating" is noted on a separate flap.*

* 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.