Epinephrine Injection, Solution
Product Images NDC 51662-1476

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Epinephrine (NDC 51662-1476). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

0.1 mg 2 Pack And Trainer Box (0.1 mg 2 Pack And Trainer Box)

0.1 mg 2 Pack And Trainer Box (0.1 mg 2 Pack And Trainer Box)
Epinephrine injection USP is a recommended medication for patients weighing between 16.5 to 33 Ibs. It comes in the form of an auto-injector that dispenses a single dose and needs to be refilled after use. The medication contains adrenaline, sodium chloride, sodium bisulfite, and water for injection. The injection trainer provided with the medication does not contain active drugs or needles. The medication should be protected from heat and light and should be stored at room temperature. In case of solution discoloration, cloudiness, or particles, replace the auto-injector. The product should not be refrigerated or frozen, and the pharmacist should dispense the entire kit as a unit.*
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0.1 mg 2 Pack And Trainer Serialized Carton (0.1 mg 2 Pack And Trainer Serialized Box)

0.1 mg 2 Pack And Trainer Serialized Carton (0.1 mg 2 Pack And Trainer Serialized Box)
Auvi-q® is an epinephrine injection, USP, auto-injector for allergic emergencies in patients weighing 16.5 Ib to 33 Ib. This product is RX-only and has the NDC code 60842-021-01. The auto-injector is manufactured by HF Acquisition Co., LLC, and distributed by Mukilteo, WA 98275. Additionally, there is a warning for California residents about the batteries used in this product.*
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Injector Labeling 1 (0.1 mg Injector Labeling 1)

Injector Labeling 1 (0.1 mg Injector Labeling 1)
This appears to be a set of instructions for using an auto-injector device during an allergic emergency. The text includes steps for removing a safety guard and placing the black end against the outer thigh, followed by seeking medical attention. The device is identified by a code of "SA6026-03-04".*
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A (A)

A (A)
The text seems to be a partial description of a device called "Quarter Case". It has a viewing window and an LED light, and a red safety guard with a black base. It is unclear what specific purpose or function the device serves, as the rest of the text is not available.*
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B (B)

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C (C)

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D (D)

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Device Label

Device Label
Auvi-q is an epinephrine injection device to be used in case of allergic emergencies. The device is an auto-injector that should be handled according to the instructions on the label. The RED safety guard must be removed before use, and the BLACK end should be placed against the OUTER THIGH, and then pushed firmly and held for two seconds. After using it, medical attention should be sought.*
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E (E)

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Injector Labeling 2 (Injector Labeling 2)

Injector Labeling 2 (Injector Labeling 2)
This is a prescription drug labeled with the NDC code 60842-021-01 and the product code SA6017-03-04. The drug is epinephrine injection, which comes in a 0.2mg auto-injector. The label advises users not to freeze or refrigerate the product, as well as to protect it from heat and light. It should be stored at room temperature between 68° and 77°F (20° to 25°C), with excursions permitted to 59° to 86°F (15° t0 30°C). Users should replace the auto-injector if the solution is discolored, cloudy, or contains particles.*
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Outer Case Labeling

Outer Case Labeling
This is a description of a medication auto-injector containing 0.1 mg of epinephrine injection in a labeled outer case. The label provides instructions that the auto-injector should not be frozen or refrigerated but instead kept at room temperature between 68°F-77°F (20°C-25°C). Temperature excursions up to 59°F-86°F (15°C-30°C) are permitted. The user should replace the auto-injector if the solution appears discolored, cloudy, or contains particles.*
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Structure (Structure)

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Serialized Label 1 Pack

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Trainer Instructions (Trainer Inst)

Trainer Instructions (Trainer Inst)
The TRAINER for AUVI-Q is a device that does not contain a needle or medicine, and it is intended to be used for practicing injections in case of an allergic emergency. It looks like the real AUVI-Q and has voice instructions and blinking red and green lights, making it easy to use. The TRAINER for AUVI-Q should be practiced daily for the first week after receiving it to prepare the user to use the AUVI-Q safely in an emergency. Practicing with the TRAINER involves pulling off the red safety guard, placing the black end against the middle of the outer thigh, pushing it until a clicking and hissing sound is heard, and holding it in place for two seconds. After practicing, the TRAINER must be reset.*

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