Auvi-q Injection, Solution
Product Images NDC 71872-7173

View Photos of 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 71872-7173). 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

71872-7173-1 Pdp (7173)

71872-7173-1 Pdp (7173)
This is a description of the Auvi-Q epinephrine Injection, USP prefilled auto-injector, which is used during allergic emergencies for patients weighing over 66 lb. The injector contains 0.3 mg epinephrine and needs to be refilled after single use. An enclosed patient information leaflet should be read before using it. The auto-injector should not be refrigerated or frozen, and should also be protected from heat and light. It should also be discarded if solution is discolored, cloudy or contains particles. The injector must be stored at room temperature and excursions are permitted to 86°F. It is manufactured by kaleo, inc. in Germany, and distributed by Modicel Purchasing Solutions.*
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Chemical Structure (Auvi Q 01)

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Figure A (Auvi Q 02)

Figure A (Auvi Q 02)
This text appears to be describing a device's outer case, which features a viewing window and a red safety guard. There is a black needle end and a base. However, it is not clear what type of device this is.*
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Figure B (Auvi Q 03)

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Figure C (Auvi Q 04)

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Figure D (Auvi Q 05)

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Figure E (Auvi Q 06)

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Figure A1 (Auvi Q 07)

Figure A1 (Auvi Q 07)
This document likely refers to a product container or packaging, possibly for electronics. It appears to have an outer case, with the brand name TRRINER and the mention of LEDs, possibly indicating lighting features. The base is also mentioned, along with a "Safety Guard" which may be a safety feature on the product.*
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Figure A2 (Auvi Q 08)

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Figure A3 (Auvi Q 09)

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Figure A4 (Auvi Q 10)

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Figure A5 (Auvi Q 11)

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Figure B (Auvi Q 12)

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Figure C (Auvi Q 13)

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Figure D (Auvi Q 14)

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Figure E (Auvi Q 15)

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Figure F (Auvi Q 16)

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Figure G (Auvi Q 17)

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0.3 mg Outer Case Label (Auvi Q 19)

0.3 mg Outer Case Label (Auvi Q 19)
This is a medication with NDC code 60842-023-01 for allergic emergencies. It should not be refrigerated or frozen, but rather protected from heat and light and stored at room temperature between 68° to 77°F (20° to 25°C) with excursions permitted to 59° to 86°F (15° to 30°C). The auto-injector solution needs to be replaced if discolored, cloudy, or containing particles. There are instructions for use inside the device, and the medication was manufactured in Germany by INO-HAL.*
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0.3 mg Device Label (Auvi Q 20)

0.3 mg Device Label (Auvi Q 20)
This is a set of instructions for using an epinephrine auto-injector in case of allergic emergencies. The user is instructed to remove the red safety guard, position the black end against the outer thigh and push firmly for two seconds. After using, the user should seek medical attention and refill the prescription. It is recommended to replace the outer case and dispose of the used injector properly.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.