Auvi-q Injection, Solution
Product Images NDC 71872-7172

20 FDA label images from Medical Purchasing Solutions, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 20 technical images submitted to the FDA as part of the official labeling for Auvi-q (NDC 71872-7172). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, Llc, 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

71872-7172-1 Pdp (7172)

71872-7172-1 Pdp (7172)
Label for Auvi-Q epinephrine Injection, USP 0.15 mg/0.15 mL prefilled auto-injector. The label includes dosage form as injection solution for intramuscular use, quantity of 1 injector, and instructions for allergic emergencies. It notes storage conditions and manufacturer information: produced by kaleo, Inc. in Richmond, VA, with repackaging and distribution by Medical Purchasing Solutions, LLC in Scottsdale, AZ. The label also displays the product NDC 71872-7172-1.*
FDA Label Image

Chemical Structure (Auvi Q 01)

Chemical Structure (Auvi Q 01)
Chemical structure of epinephrine, showing a benzene ring with three hydroxyl groups and an attached side chain including a methylated amine group.*
FDA Label Image

Figure A (Auvi Q 02)

Figure A (Auvi Q 02)
Illustration showing components of the Auvi-Q epinephrine injection device and its outer case. The device features a speaker, LED lights, viewing window, red safety guard at the needle end, and black base. The outer case is depicted with a blue top and a green arrow on the front.*
FDA Label Image

Figure B (Auvi Q 03)

Figure B (Auvi Q 03)
An instructional illustration showing hands holding the Auvi-Q epinephrine injection device. The image depicts directional arrows indicating the motion to remove the outer case, guiding user interaction with the autoinjector. No text or dosage information is visible in this image.*
FDA Label Image

Figure C (Auvi Q 04)

Figure C (Auvi Q 04)
An instructional illustration showing a hand holding an Auvi-Q epinephrine injection device. The image depicts proper positioning of the device against the outer thigh for intramuscular injection, with arrows indicating the direction to press the device firmly into the thigh for administration.*
FDA Label Image

Figure D (Auvi Q 05)

Figure D (Auvi Q 05)
An instructional illustration showing a person holding the Auvi-Q epinephrine injection device with an arrow indicating the motion to press against the thigh. Next to this, a stopwatch graphic displays a 5-second countdown with '2 seconds' marked in red, depicting the required injection duration for the .15 mg dose via intramuscular route.*
FDA Label Image

Figure E (Auvi Q 06)

Figure E (Auvi Q 06)
An instructional illustration showing a hand holding an Auvi-Q epinephrine injection device against an arm with a target symbol. Next to it, a stopwatch graphic indicates a 2-second duration, demonstrating the proper injection time for the intramuscular epinephrine solution.*
FDA Label Image

Figure A1 (Auvi Q 07)

Figure A1 (Auvi Q 07)
Illustration showing the outer case and a trainer device for Auvi-Q epinephrine injection, 0.15 mg/0.15 mL. The outer case is labeled for storing the trainer. The device is labeled with parts including speaker, housing, LEDs, base, and safety guard, and is used for practice only, not for actual injection.*
FDA Label Image

Figure A2 (Auvi Q 08)

Figure A2 (Auvi Q 08)
Auvi-Q Trainer injection, solution carton packaging for training purposes. The carton is primarily white and black with the word 'TRAINER' prominently displayed on the top and sides, indicating it is a non-medicated practice device. Manufactured by Medical Purchasing Solutions, LLC.*
FDA Label Image

Figure A3 (Auvi Q 09)

Figure A3 (Auvi Q 09)
Auvi-Q 0.15 mg/.15 mL epinephrine injection solution in an intramuscular autoinjector device. The image shows the front and back of the Auvi-Q injector with red and white labeling, including usage instructions and warnings. The product is labeled by Medical Purchasing Solutions, LLC.*
FDA Label Image

Figure A4 (Auvi Q 10)

Figure A4 (Auvi Q 10)
The image shows the Auvi-Q 0.15 mg epinephrine injection, solution, intramuscular device packaging and its accompanying instructions label. The front of the device is blue with white and yellow text, displaying the proprietary name Auvi-Q, generic name epinephrine injection USP, and strength 0.15 mg injection. The labeler is Medical Purchasing Solutions, LLC. The back label provides step-by-step illustrated instructions for use, including pulling the yellow safety guard, removing the device cap, and administering the injection intramuscularly.*
FDA Label Image

Figure A5 (Auvi Q 11)

Figure A5 (Auvi Q 11)
Auvi-Q 0.15 mg epinephrine injection, solution, auto-injector label showing front and back views. The front includes product name, generic name, dosage strength, and administration route. The back features step-by-step illustrated instructions for intramuscular injection, including device removal, injection process, and emergency use directions. Labeler is Medical Purchasing Solutions, LLC.*
FDA Label Image

Figure B (Auvi Q 12)

Figure B (Auvi Q 12)
An instructional illustration showing a person holding an Auvi-Q device, demonstrating how to slide the outer case up and down with arrows indicating the direction of movement. This diagram is part of the administration instructions for the Auvi-Q epinephrine injection device.*
FDA Label Image

Figure C (Auvi Q 13)

Figure C (Auvi Q 13)
An instructional illustration showing a hand holding an Auvi-Q epinephrine injection device and pressing the device down onto a finger with directional arrows indicating the motion required to activate the injection.*
FDA Label Image

Figure D (Auvi Q 14)

Figure D (Auvi Q 14)
An instructional illustration showing how to hold and administer Auvi-Q epinephrine injection intramuscularly. The image depicts a hand gripping the device against the thigh with an arrow indicating the pressing motion. Next to it is a stopwatch graphic emphasizing a 2-second administration time.*
FDA Label Image

Figure E (Auvi Q 15)

Figure E (Auvi Q 15)
An instructional illustration showing a pair of hands holding an Auvi-Q epinephrine autoinjector device near a person's outer thigh, indicating the proper intramuscular injection site. The image uses red target-like markings to highlight the injection area on the thigh.*
FDA Label Image

Figure F (Auvi Q 16)

Figure F (Auvi Q 16)
An instructional illustration showing a hand holding an Auvi-Q epinephrine injection device with arrows indicating to not hold the black base while inserting the red safety guard. The image guides proper handling during the preparation for intramuscular injection.*
FDA Label Image

Figure G (Auvi Q 17)

Figure G (Auvi Q 17)
An instructional illustration showing a hand holding an Auvi-Q epinephrine injection device. Arrows indicate steps to operate the device, suggesting where to press and pull to use the injection for intramuscular administration.*
FDA Label Image

0.15 mg Outer Case Label (Auvi Q 22)

0.15 mg Outer Case Label (Auvi Q 22)
The image is a packaging label for Auvi-Q epinephrine injection, USP 0.15 mg auto-injector. The blue label features usage instructions indicating it is for single-use and for allergic emergencies in patients weighing 33 to 66 pounds. It includes storage instructions and cautions not to refrigerate or freeze. The label states it is manufactured for kaleo, with origin Germany.*
FDA Label Image

0.15 mg Device Label (Auvi Q 23)

0.15 mg Device Label (Auvi Q 23)
Instructional diagram for Auvi-Q epinephrine injection 0.15 mg auto-injector showing steps for use in allergic emergencies. The label guides pulling the red safety guard, placing the black end against the outer thigh, and pushing firmly for 2 seconds, with a recommendation to seek medical attention afterwards. Manufacturer is listed as kaleo, Inc.*

* 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.