Zegerid Powder, For Suspension
Product Images NDC 68012-052

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Zegerid (NDC 68012-052). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Santarus, 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

Image 01

Image 01
Chemical structure diagram of omeprazole, the active ingredient in ZEGERID. The diagram shows the molecular framework including heterocyclic rings, sulfur and nitrogen atoms, and methoxy groups consistent with omeprazole's chemical makeup.*
FDA Label Image

Image 02

Image 02
Packaging label for Zegerid 20 mg/1,680 mg powder for oral suspension. The label displays the proprietary product name Zegerid with active ingredients omeprazole and sodium bicarbonate. It indicates the oral suspension dosage form and strength of 20 mg omeprazole and 1,680 mg sodium bicarbonate per unit. The label includes distributor and manufacturer information for Salix Pharmaceuticals and contains a barcode. There is a note to pharmacists to dispense the enclosed medication guide and a space for placing the prescription label.*
FDA Label Image

Image 03

Image 03
Packaging label for Zegerid 40 mg/1,680 mg powder for oral suspension containing omeprazole and sodium bicarbonate. The label indicates it is for prescription use only, distributed by Salix Pharmaceuticals and manufactured by PTI Royston, LLC. The label includes dosage instructions, pharmacist dispensing guidance, and contact information, with a space for a prescription label.*
FDA Label Image

Image 04

Image 04
Zegerid capsules containing 20 mg omeprazole and 1,100 mg sodium bicarbonate are displayed on this label. The packaging contains 30 capsules and is produced by Santarus, Inc. The label includes a barcode, dosage instructions, storage conditions, distributor information, and a phone number for further information.*
FDA Label Image

Image 05

Image 05
ZEGERID capsules label showing the proprietary name and active ingredients omeprazole and sodium bicarbonate. The label indicates a strength of 40 mg/1,100 mg and a quantity of 30 capsules. Additional text includes dosing information, storage conditions, distributor details, trademark and copyright notices, and a customer contact phone number.*

* 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.