E-z-paque Suspension
Product Images NDC 32909-187

3 FDA label images from E-z-em Canada Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for E-z-paque (NDC 32909-187). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by E-z-em Canada 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.

Product Images & Figures Index

FDA Label Image

Liquid E Z Paque External Label

Liquid E Z Paque External Label
Liquid E-Z-PAQUE (Barium Sulfate) Oral Suspension 0.6 g/mL in a single-dose 355 mL bottle by E-Z-EM Canada Inc. The label indicates it is for oral use only, for single contrast GI studies, with storage and usage instructions. It includes inactive ingredient details and a barcode.*
FDA Label Image

Liquid E Z Paque Internal Label

Liquid E Z Paque Internal Label
The label for Liquid E-Z-PAQUE oral suspension, containing 0.6 g/mL barium sulfate. This single-dose bottle label is for use in radiographic examinations of the esophagus, stomach, and small bowel. It includes storage instructions, manufacturer information (E-Z-EM Canada Inc), and a barcode. The label also contains inactive ingredient details and lot/expiry areas.*
FDA Label Image

Barium-sulfate-structure (Barium Sulfate Structure)

Barium-sulfate-structure (Barium Sulfate Structure)
Chemical structure diagram showing the sulfate ion paired with a Ba2+ (barium) cation, indicating the chemical composition relevant to E-Z-Paque. The structure depicts the sulfate ion with four oxygen atoms around a sulfur atom and an overall 2- charge.*

* 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.