Albuterol Sulfate Solution
Product Images NDC 55154-2132

View Photos of 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 Albuterol Sulfate (NDC 55154-2132). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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.

FDA Label Image

Bag Label (6ec88f64 66a2 4ca9 9913 C192fc33f88b 00)

Bag Label (6ec88f64 66a2 4ca9 9913 C192fc33f88b 00)
Albuterol Sulfate Inhalation Solution 2.5 mg/3 mL in a package of 5 x 3 mL sterile unit-dose vials, each vial containing 0.083% albuterol equivalent to 3 mg albuterol sulfate. Label indicates for oral inhalation only, RX only, no preservatives, and storage instructions to keep between 2° and 25°C. Manufactured by The Ritedose Corporation and distributed by Cardinal Health and American Health Packaging.*
FDA Label Image

Chemical Structure (Albuterol 01)

Chemical Structure (Albuterol 01)
Chemical structure of Albuterol Sulfate showing the molecular arrangement including a benzene ring with hydroxyl groups, an alcohol side chain, and a sulfate component. This structure corresponds to the active ingredient Albuterol Sulfate.*
FDA Label Image

Figures (Albuterol 02)

Figures (Albuterol 02)
An instructional diagram showing three steps for using a respiratory inhalation solution device. The first panel depicts filling or preparing the device. The second panel shows attaching or adjusting parts of the inhaler. The third panel illustrates a person administering the inhalation from the device.*

* 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.