Pulmicort Aerosol, Powder
Product Images NDC 50090-7867

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Pulmicort (NDC 50090-7867). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Image Description (Image 01)

Chemical structure diagram showing the molecular structure of Budesonide, the active ingredient in PULMICORT FLEXHALER. The diagram depicts atom connectivity and stereochemistry of the compound.*

FDA Label Image

Image Description (Image 02)

A line graph depicting change in FEV1 (L) over 12 weeks comparing PULMICORT FLEXHALER 180 mcg (2 inhalations twice daily), PULMICORT TURBUHALER 200 mcg (2 inhalations twice daily), and placebo. The graph shows increases in FEV1 for both active treatments versus placebo, with data points at weeks 0, 2, 4, 8, and 12 and sample sizes noted for each time point.*

FDA Label Image

Image Description (Image 03)

A line graph depicting the change in predicted FEV1 percentage over a 12-week treatment period for three groups: PULMICORT FLEXHALER 90 mcg (4 inhalations twice daily), PULMICORT TURBUHALER 200 mcg (2 inhalations twice daily), and placebo. The x-axis represents weeks, while the y-axis shows percentage change in predicted FEV1. Data points show increasing FEV1 changes for both active treatments compared to placebo over time.*

FDA Label Image

Image Description (Image 04)

An instructional diagram showing the parts of a Pulmicort Flexhaler inhalation device. It labels the mouthpiece at the top, the dose indicator in the middle, the brown grip at the bottom, and a separate cover piece placed next to the inhaler.*

FDA Label Image

Image Description (Image 05)

An instructional line drawing depicting hands operating an inhaler. The image shows one hand holding the inhaler device and the other hand preparing it for use by pulling or twisting parts of the inhaler, illustrating steps to ready the aerosol powder device for respiratory inhalation.*

FDA Label Image

Image Description (Image 06)

An instructional line drawing showing hands holding a Pulmicort Flexhaler inhaler, with arrows indicating a twisting motion. The image demonstrates how to twist the inhaler to prepare it for use.*

FDA Label Image

Image Description (Image 07)

An instructional illustration showing a person holding the PULMICORT FLEXHALER inhalation device. The image demonstrates the user gripping and preparing the inhaler for use, indicating a 'Click' step to activate or load the dose.*

FDA Label Image

Image Description (Image 08)

An instructional illustration showing a person using the Pulmicort Flexhaler inhaler device. The image depicts the inhalation step, with the device held near the mouth as the user inhales the aerosol powder medication.*

FDA Label Image

Image Description (Image 09)

An instructional diagram showing a close-up of a PULMICORT FLEXHALER inhaler. The image focuses on the mouthpiece area marked with dose intervals such as 100 and 120, likely indicating dose counts or settings.*

FDA Label Image

Image Description (Image 10)

A line drawing illustration showing a dosing counter window on a Pulmicort Flexhaler inhaler device. The dosage indicator displays the number '20', representing remaining doses.*

FDA Label Image

Label Image (Lbl500907867)

PULMICORT FLEXHALER 180 mcg/actuation aerosol powder inhaler label by A-S Medication Solutions. The label includes product number 5928-0, dosage instructions to see package insert, storage conditions between 68 and 77 degrees Fahrenheit, and a count of 120 metered doses. Distributed by A-S Medication Solutions, Libertyville, Illinois.*

* 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.