Albuterol Sulfate Aerosol, Metered
Product Images NDC 0054-0742

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Albuterol Sulfate (NDC 0054-0742). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Fig-a (Albuterolfiga)

An instructional diagram showing a side and top view of an Albuterol Sulfate metered dose inhaler. The side view labels the dose indicator, canister, actuator, mouthpiece, and cap. The top view illustrates the dose indicator display window, pointer, and press here area.*

FDA Label Image

Fig-b (Albuterolfigb)

An illustration showing the top view of an inhaler actuator with a dose counter displaying the number 20, indicating the remaining doses in the container.*

FDA Label Image

Fig-c (Albuterolfigc)

An instructional diagram showing two hands holding an Albuterol Sulfate aerosol inhaler. One hand holds the inhaler in an upright position with the mouthpiece visible, while the other hand is removing the cap from the mouthpiece. The diagram labels the 'Mouthpiece,' 'Cap,' and indicates the 'Upright Position.'*

FDA Label Image

Fig-d (Albuterolfigd)

An instructional illustration showing a person using an aerosol metered-dose inhaler by placing it in their mouth and pressing down to release the medicine while inhaling.*

FDA Label Image

Fig-e (Albuterolfige)

An instructional diagram showing a hand holding an inhaler under running water from a faucet, with the inhaler being rinsed. To the right, a small cap or container is displayed upside down, suggesting cleaning or rinsing instructions for the aerosol metered inhaler device.*

FDA Label Image

Fig-f (Albuterolfigf)

An instructional illustration showing correct and incorrect use of a respiratory inhaler. The top image, labeled 'not blocked,' depicts a hand pressing the inhaler with properly releasing aerosol spray. The bottom image, labeled 'blocked,' shows the inhaler nozzle being obstructed, causing improper medication release.*

FDA Label Image

Fig-g (Albuterolfigg)

An illustration divided into two sections: the top section shows a window with curtains and a crescent moon outside, suggesting nighttime or evening. The bottom section depicts an inhaler device, a small bottle with dropper, and a round cap, representing common respiratory inhalation devices and medication containers.*

FDA Label Image

Fev1 Graph (Albuterolgraphfinal)

A line graph showing the percent change in FEV1 from predose over 6 hours during a large 12-week clinical trial. The graph compares three treatments: Albuterol Sulfate inhalation aerosol (2 puffs, 4 times daily), CFC 11/12 Albuterol (2 puffs, 4 times daily), and HFA-134a placebo (2 puffs, 4 times daily). Percent change in FEV1 is plotted on the vertical axis and time in hours on the horizontal axis.*

FDA Label Image

Label (Albuterollabel)

Label for Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, metered aerosol dosage form for respiratory inhalation. The label indicates 200 metered inhalations per container, contains no chlorofluorocarbons, and is marked for prescription use only. It includes usage warnings, storage instructions, and lists Hikma Pharmaceuticals USA Inc. as the distributor and Aeropharm GmbH as the manufacturer.*

FDA Label Image

Chemical Structure (Albuterolsulfatechemicalstructure)

Chemical structure of Albuterol Sulfate showing two sulfate ions and the organic molecular structure with hydroxyl groups and an amine group, consistent with its formula.*

* 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.