Qvar Redihaler Aerosol, Metered
Product Images NDC 50090-3458

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Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Qvar Redihaler (NDC 50090-3458). 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, the active ingredient in QVAR REDIHALER. The diagram depicts the molecular arrangement with labeled functional groups, including ester and hydroxyl groups, consistent with corticosteroid compounds.*
FDA Label Image

Figure F (Image 10)

Figure F (Image 10)
An instructional illustration showing a person removing the cap from a QVAR REDIHALER metered dose inhaler. The image demonstrates proper handling of the aerosol inhaler device for respiratory administration.*
FDA Label Image

Teva Logo (Image 11)

FDA Label Image

Figure 1 (Image 2)

Figure 1 (Image 2)
Line graph showing FEV1 change from baseline (liters) over time (weeks) in a clinical study. The graph compares QVAR REDIHALER 80 mcg/day, QVAR REDIHALER 160 mcg/day, and placebo groups at baseline, 2, 4, 8, and 12 weeks. Data points include mean changes with error bars for variability.*
FDA Label Image

Figure 2 (Image 3)

Figure 2 (Image 3)
A line graph showing FEV1 change from baseline (in liters) over time (weeks) for four treatment groups: QVAR REDIHALER 320 mcg/day, QVAR REDIHALER 640 mcg/day, QVAR MDI 320 mcg/day, and placebo. The graph plots FEV1 changes at baseline, week 2, week 4, and week 6, with error bars indicating variability.*
FDA Label Image

Teva Respiratory Logo (Image 4)

FDA Label Image

Figure A (Image 5)

Figure A (Image 5)
An instructional diagram of a QVAR REDIHALER inhaler showing labeled parts: Vent at the top, Mouthpiece in the middle, and White Cap at the bottom. The image depicts key components for respiratory inhalation use.*
FDA Label Image

Figure B (Image 6)

Figure B (Image 6)
Illustration of a dose counter on a QVAR REDIHALER (Beclomethasone Dipropionate HFA) metered aerosol inhaler. The image shows the dose counter indicating a full inhaler with 120 doses remaining and an empty inhaler with 0 doses, highlighting the dose counter display detail on the device's base.*
FDA Label Image

Figure C (Image 7)

Figure C (Image 7)
An instructional illustration showing hands operating a QVAR REDIHALER metered dose inhaler. The image highlights the action of clicking the top part of the inhaler to use it, with an arrow and the word "Click!" indicating the movement.*
FDA Label Image

Figure D (Image 8)

Figure D (Image 8)
Illustration showing how to open the mouthpiece cover of a QVAR REDIHALER aerosol inhaler. The image depicts hands removing the cap by pulling it downward, demonstrating the device’s use for respiratory inhalation of Beclomethasone Dipropionate HFA.*
FDA Label Image

Figure E (Image 9)

Figure E (Image 9)
An instructional illustration showing a person using a QVAR REDIHALER aerosol inhaler. The image depicts the inhaler being placed near the mouth, with an arrow indicating the direction of inhalation activation by pressing down on the canister. The diagram emphasizes correct inhaler use technique for respiratory administration.*
FDA Label Image

Label Image (Lbl500903459)

Label Image (Lbl500903459)
Label for QVAR REDIHALER containing Beclomethasone Dipropionate HFA aerosol, metered inhalation with 120 metered inhalations per container. The label includes the NDC 50090-3459-0 and product number 6786-0. It is distributed by A-S Medication Solutions in Libertyville, IL.*

* 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.