Albuterol Sulfate Solution
Product Images NDC 55154-4410

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Albuterol Sulfate (NDC 55154-4410). 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 (D2132c1c 0f90 4c6f Afc0 F3814b6a7e5c 00)

Bag Label (D2132c1c 0f90 4c6f Afc0 F3814b6a7e5c 00)
This text panel provides detailed prescribing information for Albuterol Sulfate Inhalation Solution 2.5 mg/3 mL, supplied as sterile unit-dose vials in foil pouches by Cardinal Health. It includes dosage instructions, preparation steps for administration via nebulizer, storage conditions, and safety precautions including restricted use for institutional settings.*
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 hydroxy and hydroxymethyl groups, and the sulfate salt form.*
FDA Label Image

Figures (Albuterol 02)

Figures (Albuterol 02)
An instructional diagram showing three steps for using an inhalation device with Albuterol Sulfate solution. Step 1 depicts assembling the device, Step 2 shows inserting a component, and Step 3 illustrates a person inhaling through the device.*
FDA Label Image
Rdp Logo (Rdp Logo)
Albuterol Sulfate 2.5 mg/3 mL solution for respiratory inhalation by Cardinal Health 107, LLC, shown in a clear plastic ampule with labeling. The ampule is individually packaged for single use, intended for inhalation therapy.*

* 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.