Pulmicort
Product Images NDC 21695-291

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Pulmicort (NDC 21695-291). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Structural Formula (0950cd08 A48b 4376 9647 Da22cf5a8a70 01)

Chemical structure diagram depicting the active ingredient(s) found in PULMICORT FLEXHALER by Rebel Distributors Corp. The structure shows a steroidal backbone with multiple rings and functional groups, along with an additional smaller chemical structure on the right side of the image.*

FDA Label Image

Figure 1 (0950cd08 A48b 4376 9647 Da22cf5a8a70 02)

A line graph showing the change in FEV1 (L) over a 12-week period comparing three treatments: PULMICORT FLEXHALER 180 mcg, PULMICORT TURBUHALER 200 mcg, and placebo. The graph includes data points at multiple weeks and indicates a greater improvement in FEV1 for the PULMICORT FLEXHALER group compared to the other groups.*

FDA Label Image

Figure 2 (0950cd08 A48b 4376 9647 Da22cf5a8a70 03)

A line graph comparing the percentage change in predicted FEV1 over 12 weeks among three groups: PULMICORT FLEXHALER 90 mcg (4 inhalations twice daily), PULMICORT TURBUHALER 200 mcg (2 inhalations twice daily), and placebo. The y-axis shows the change in % predicted FEV1, and the x-axis shows time in weeks. Data points indicate that both active treatments improved FEV1 more than placebo, with FLEXHALER showing the highest increase.*

FDA Label Image

Figure 1 (0950cd08 A48b 4376 9647 Da22cf5a8a70 04)

An instructional diagram showing the parts of a Pulmicort Flexhaler inhaler. It labels the mouthpiece, dose indicator, brown grip, and the removable cover. The diagram visually identifies each component of the device for user reference.*

FDA Label Image

Figure 2 (0950cd08 A48b 4376 9647 Da22cf5a8a70 05)

Illustration showing a person's hand holding a Pulmicort Flexhaler device and twisting the bottom to prepare a dose. This instructional image demonstrates the proper technique to activate the inhaler before use.*

FDA Label Image

Figure 3 (0950cd08 A48b 4376 9647 Da22cf5a8a70 06)

An instructional illustration showing how to hold and twist the base of a Pulmicort Flexhaler device. The image demonstrates proper hand positioning and the twisting motion needed to activate the inhaler.*

FDA Label Image

Figure 4 (0950cd08 A48b 4376 9647 Da22cf5a8a70 07)

An instructional diagram showing how to use the Pulmicort Flexhaler inhaler. It demonstrates holding the inhaler upright with one hand while twisting the base with the other hand until a 'click' is felt, indicating the dose is ready for use.*

FDA Label Image

Figure 5 (0950cd08 A48b 4376 9647 Da22cf5a8a70 08)

Instructional illustration showing how to use the PULMICORT FLEXHALER inhaler device. The image depicts a person holding the inhaler near their mouth, exhaling, and preparing to inhale the medication. The text 'Inhale' appears below the image.*

FDA Label Image

Figure 6 (0950cd08 A48b 4376 9647 Da22cf5a8a70 09)

An illustration showing the dial or dose counter on the PULMICORT FLEXHALER device, indicating the remaining doses with numbers 100 and 120 clearly visible. The image depicts part of the device used to administer the medication.*

FDA Label Image

Figure 7 (0950cd08 A48b 4376 9647 Da22cf5a8a70 10)

An illustration showing a dose counter window on a device, with visible numbers '21' and '20' indicating the remaining doses. The image is related to the PULMICORT FLEXHALER inhalation device.*

FDA Label Image

Pulmicort Flexhaler 90mcg (0950cd08 A48b 4376 9647 Da22cf5a8a70 11)

Label for Pulmicort Flexhaler 90 mcg #1 (60 doses) inhaler showing dosage strength and form. The label indicates each metered dose contains 90 mcg. It includes NDC 21695-291-01 and notes the manufacturer as AstraZeneca AB, Sodertalje, Sweden. The label also states it is for RX only and provides storage instructions with distributor information for Physician Partner, Thousand Oaks, CA.*

* 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.