Albuterol Sulfate
Product Images NDC 68071-5206

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Albuterol Sulfate (NDC 68071-5206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,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

Pdp (68071 5206 2)

Label for Albuterol Sulfate 200 Metered Inhaler by NuCare Pharmaceuticals, Inc. The label includes NDC 68071-5206-2 and states each actuation delivers 108 mcg Albuterol Sulfate, equivalent to 90 mcg Albuterol from the mouthpiece. It features dosage instructions, warnings to keep out of reach of children, storage temperature guidelines, and manufacturer details.*

FDA Label Image

Chemical-structure (Chemical Structure)

Chemical structure diagram of albuterol sulfate, illustrating the molecular components including hydroxyl groups, an amine group, and sulfate ion association.*

FDA Label Image

Figure-a-b.jpg (Figure A B)

Diagram illustrating the components of an albuterol sulfate inhaler by NuCare Pharmaceuticals, Inc. Figure A labels the metal canister, plastic actuator, mouthpiece, and cap. Figure B highlights the dose counter located on the inhaler cap, showing the number 203.*

FDA Label Image

Figure-c.jpg (Figure C)

Illustration depicting a person holding an albuterol sulfate inhaler with a spacer device near the mouth, demonstrating correct use for inhalation. The image highlights proper positioning of the inhaler and spacer in preparation for medication administration.*

FDA Label Image

Figure-d.jpg (Figure D)

An instructional diagram titled 'Figure D' showing the priming process for albuterol sulfate inhalation aerosol. It depicts two spray counters: one reading 203 sprays before priming and another reading 200 sprays after priming, with an arrow labeled 'PRIMING' between them, explaining the change in the spray counter during device priming.*

FDA Label Image

Figure-e.jpg (Figure E)

An instructional illustration showing the proper handling of an inhaler by NuCare Pharmaceuticals, Inc. It depicts a hand placing the cap on the mouthpiece in the down position, labeled accordingly with arrows pointing to the mouthpiece and cap components.*

FDA Label Image

Figure-f.jpg (Figure F)

An instructional illustration showing a person using an inhaler by pushing down on the canister and breathing in. The text above the image reads, 'Push down and breathe in.' This figure is labeled as 'Figure F.'*

FDA Label Image

Figure-g-h.jpg (Figure G H)

Illustration showing the correct and incorrect blocking of an albuterol sulfate inhaler mouthpiece. Figure G demonstrates the mouthpiece blocked, preventing medicine release. Figure H shows the mouthpiece not blocked, allowing medicine to be delivered as intended.*

FDA Label Image

Figure-graphs (Figure Graphs)

Two line graphs showing mean percent change in FEV1 from pre-dose over 6 hours for a 6-week clinical trial. The top graph depicts Day 1, the bottom graph Day 43. Each graph compares albuterol sulfate inhalation aerosol, matched placebo HFA inhalation aerosol, and marketed HFA-134a albuterol inhaler with sample sizes indicated. Axes show percent change in FEV1 and time in hours.*

FDA Label Image

Figure-i.jpg (Figure I)

Illustration showing a hand holding an inhaler mouthpiece being washed under warm running water. The image includes text instructing to "Wash Mouthpiece under warm running water." This is labeled as Figure I.*

FDA Label Image

Figure-j.jpg (Figure J)

An instructional illustration labeled Figure J showing a person holding and rinsing an albuterol sulfate inhaler mouthpiece under a running faucet, demonstrating how to clean the device.*

FDA Label Image

Figure-k.jpg (Figure K)

An instructional illustration labeled 'Figure K' depicting guidance on allowing a mouthpiece to dry overnight. The image includes a depiction of a mouthpiece and a device, set against a nighttime window background with a crescent moon and star.*

* 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.