Varibar Nectar Suspension
Product Images NDC 32909-116

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 Varibar Nectar (NDC 32909-116). 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.

FDA Label Image

Barium-sulfate-structure (Barium Sulfate Structure)

Barium-sulfate-structure (Barium Sulfate Structure)
Chemical structure of barium sulfate, represented with a barium ion (Ba2+) and a sulfate ion (SO4 2-). This structure is commonly associated with the active ingredient in Varibar Nectar 400 mg/mL, a diagnostic agent by E-Z-EM Canada Inc.*
FDA Label Image

Varibar Nectar Internal Label

Varibar Nectar Internal Label
Varibar Nectar 400 mg/mL (Barium Sulfate) oral suspension 40% w/v in a 240 mL container. The label indicates it is for oral use only and prescription use. It is manufactured for Bracco Diagnostics Inc. and distributed by E-Z-EM Canada Inc. The label includes storage instructions, usage directions, and a detailed list of inactive ingredients.*
FDA Label Image

Varibar-nectar-internal-label (Varibar Nectar Internal Label)

Varibar-nectar-internal-label (Varibar Nectar Internal Label)
Varibar Nectar 400 mg/mL oral suspension label, a barium sulfate preparation by E-Z-EM Canada Inc for Bracco Diagnostics Inc. The label states it is a multiple-unit container for oral use, intended for modified barium swallow examinations. The suspension concentration is 40% w/v, packaged in a 240 mL container. Storage instructions and barcode are also present.*

* 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.