Epinephrine 0.3 Adults Injection
Product Images NDC 70385-2022

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Epinephrine 0.3 Adults (NDC 70385-2022). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sina Health 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

Chemical Structure (Epinephrine Injection 1)

Chemical structure diagram of Epinephrine showing its molecular arrangement with hydroxyl groups and amine side chain.*

FDA Label Image

1 (Epinephrine Injection 10)

Packaging label for Epinephrine 0.3 Adults injection auto-injector by Sina Health Inc. The label includes instructions for use, dosage strength of 0.15 mg epinephrine per 0.3 mL, and manufacturer information. The label features step-by-step illustrations on administering the injection and proper disposal of the auto-injector after use. The label also notes storage conditions and warnings for allergic emergencies (anaphylaxis).*

FDA Label Image

0-3mg Carton (Epinephrine Injection 11)

Packaging label for Epinephrine injection, USP auto-injector 0.3 mg by Amneal Pharmaceuticals LLC. The carton states it contains two epinephrine auto-injectors for subcutaneous use in allergic emergencies. Instructions with illustrations show how to remove the injector from its case and administer the injection into the thigh. Storage and handling information is included, advising protection from heat/light and not to refrigerate.*

FDA Label Image

1 (Epinephrine Injection 12)

Packaging label for Epinephrine 0.3 mg injection auto-injector, providing 0.3 mg strength. It includes administration instructions with illustrations for pulling off blue caps, pushing the red tip firmly for 10 seconds, and seeking medical attention after use. The label states the product is for intramuscular or subcutaneous use, distributed by Amneal Pharmaceuticals LLC, with storage instructions and warnings about use and disposal.*

FDA Label Image

1 (Epinephrine Injection 2)

An instructional labeled diagram showing parts of an epinephrine auto-injector device. The diagram identifies components such as the carrying case, end caps, red tip (needle end), viewing window, and the auto-injector body. The auto-injector label indicates a strength of 0.15 mg.*

FDA Label Image

1 (Epinephrine Injection 3)

An instructional diagram of the Epinephrine 0.3 Adults auto-injector package by Sina Health Inc. It shows a black and yellow carrying case removed from a yellow protective case, with labeled parts of the auto-injector syringe including the blue end caps, red needle tip, viewing window, and auto-injector mechanism.*

FDA Label Image

Figure A (Epinephrine Injection 4)

An instructional illustration showing hands twisting and pulling apart an epinephrine injection pen. Arrows indicate the direction to twist and pull the device to prepare it for use, accompanied by the text 'Twist and Pull.' This likely demonstrates how to remove the safety cap or activate the product before injection.*

FDA Label Image

Figure B (Epinephrine Injection 5)

An instructional diagram showing a step to pull off both blue caps from a device. The image includes arrows and text indicating the direction to pull and highlights the two separate blue caps to be removed. The diagram is part of a multi-step process, denoted by the number 2 in a circle.*

FDA Label Image

Figure C (Epinephrine Injection 6)

An instructional illustration showing a hand holding an Epinephrine 0.3 Adults injection device with a red tip, being pushed firmly against a thigh. Text instructs to push the red tip hard into the thigh for 10 seconds.*

FDA Label Image

Figure D (Epinephrine Injection 7)

An instructional illustration showing two hands holding a syringe-like device. The left hand holds the device with a cap, and an arrow indicates the cap being pulled off toward the right hand's position, demonstrating how to remove the cap before injection.*

FDA Label Image

Figure E (Epinephrine Injection 8)

An instructional line drawing showing two hands holding an Epinephrine 0.3 Adults injection auto-injector. An arrow between the hands indicates the motion of sliding or removing a safety cap from the device before use.*

FDA Label Image

0-15mg Carton (Epinephrine Injection 9)

Packaging label for Epinephrine injection USP auto-injector 0.15 mg by Amneal Pharmaceuticals LLC. The label includes instructions for use, storage conditions, and a barcode. It indicates the product is for allergic emergencies in patients weighing 33 to 66 lbs, for subcutaneous or intramuscular use. The carton contains two epinephrine auto-injectors and displays the NDC 0115-1695-49.*

* 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.