Qvar Redihaler Aerosol, Metered
Product Images NDC 50090-5031

10 FDA label images from A-s Medication Solutions · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Qvar Redihaler (NDC 50090-5031). 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

Chemical Structure (Image 1)

Chemical Structure (Image 1)
Chemical structure of Beclomethasone Dipropionate as shown in the image, featuring a steroid backbone with chlorinated and ester functional groups.*
FDA Label Image

Figure 1 (Image 2)

Figure 1 (Image 2)
A line graph showing FEV1 change from baseline (in liters) over time with visits at baseline, 2, 4, 8, and 12 weeks. It compares three groups: QVAR REDIHALER 80 mcg/day, QVAR REDIHALER 160 mcg/day, and placebo. The graph displays mean values with error bars, illustrating improvement in FEV1 for both QVAR REDIHALER dosage groups compared to placebo over the 12-week period.*
FDA Label Image

Figure 2 (Image 3)

Figure 2 (Image 3)
A line graph comparing FEV1 change from baseline over 6 weeks for QVAR REDIHALER at 320 mcg/day and 640 mcg/day, QVAR MDI 320 mcg/day, and placebo groups. Time of visit is shown on the x-axis in weeks, with FEV1 change in liters on the y-axis, including error bars for variability.*
FDA Label Image

Teva Respiratory Logo (Image 4)

Teva Respiratory Logo (Image 4)
Illustration of a QVAR REDIHALER aerosol inhaler showing labeled parts: vent at the top, mouthpiece in the middle, and white cap at the bottom.*
FDA Label Image

Figure A (Image 5)

Figure A (Image 5)
An instructional illustration showing the dose counter feature of the QVAR REDIHALER aerosol inhaler. It depicts the counter display with 120 doses when full and 0 doses when empty, alongside the inhaler device itself and a close-up of the dose counter window.*
FDA Label Image

Figure B (Image 6)

Figure B (Image 6)
An instructional illustration showing hands opening or closing the mouthpiece cover of a QVAR REDIHALER aerosol inhaler with a 'Click!' sound indicated, demonstrating proper use and preparation of the inhalation device.*
FDA Label Image

Figure C (Image 7)

Figure C (Image 7)
An instructional illustration showing a person holding the QVAR REDIHALER aerosol inhaler with one hand and using the other hand to remove the cap by pulling it downward, indicated by a curved arrow. The image demonstrates the proper way to open the inhaler before use.*
FDA Label Image

Figure D (Image 8)

Figure D (Image 8)
Instructional illustration showing a person using a QVAR REDIHALER inhaler. The image depicts the inhaler being placed in the mouth with a downward arrow indicating the correct direction to tilt or press the device during administration.*
FDA Label Image

Figure E (Image 9)

Figure E (Image 9)
An instructional illustration showing an adult hand preparing a QVAR REDIHALER aerosol inhaler by lifting the mouthpiece cover upward. The image demonstrates the first step in using the inhaler device for respiratory administration of Beclomethasone Dipropionate HFA 40 mcg aerosol, metered dosage form.*
FDA Label Image

Label Image (Lbl500905031)

Label Image (Lbl500905031)
QVAR REDIHALER 40 MCG aerosol metered inhalation label by A-S Medication Solutions. The label shows the NDC 50090-5031, product number 9936-0, and states each inhalation delivers 40 micrograms of Beclomethasone Dipropionate HFA. It includes storage instructions to store at 77 degrees Fahrenheit and indicates the package contains 120 metered inhalations with a net weight of 10.6 g.*

* 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.