Epinephrine
Product Images NDC 71872-7103

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Epinephrine (NDC 71872-7103). 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

Pdp (7103)

Label text for epinephrine injection USP auto-injector 0.3 mg by Medical Purchasing Solutions, LLC. The label includes usage instructions for allergic emergencies, subcutaneous or intramuscular use, ingredients, storage conditions, expiration and lot number placeholders, distributor information, and a website for more information.*

FDA Label Image

Chemical Structure (Epinephrine Injection 1)

Chemical structure of epinephrine showing its aromatic ring, hydroxyl groups, and side chain with amine group.*

FDA Label Image

Wrap Label (0.3 mg)

Instructional label panel for epinephrine auto-injector, 0.3 mg, by Medical Purchasing Solutions, LLC, detailing preparation and administration steps with illustrations. Text advises on usage, contents per dose, storage conditions, and cautions for intramuscular or subcutaneous use in allergic emergencies (anaphylaxis). Includes manufacturer and distributor information.*

FDA Label Image

Case Label (0.3 mg)

Label for epinephrine injection USP 0.3 mg auto-injector. The label includes dosing instructions for allergic emergencies for patients over 66 lbs. It features a yellow border with a red outline and includes the instruction 'TWIST AND PULL' on the side. The label also displays the Impax logo and a revision date of 07/2016.*

FDA Label Image

Carrying Case 0.15 mg (Epinephrine Injection 2)

An instructional diagram of an epinephrine auto-injector showing its components. The auto-injector has two end caps, a red needle end tip, a viewing window, and is labeled for a 0.15 mg dose. The device is shown outside its black and orange carrying case with labeled arrows identifying each part.*

FDA Label Image

Carry Case 0.3 mg (Epinephrine Injection 3)

An illustration diagram showing a 0.3 mg epinephrine auto-injector with labeled parts. The auto-injector includes a red tip labeled 'needle end,' a blue end cap at both ends, and a viewing window for dose information. The diagram also shows a black carrying case and a separate yellow protective carrying case, both labeled accordingly.*

FDA Label Image

Figure A (Epinephrine Injection 4)

Illustration labeled as Figure A showing instructions to pull off both blue caps from a medical device associated with epinephrine. The image indicates pulling the caps in opposite directions to remove them.*

FDA Label Image

Figure B (Epinephrine Injection 5)

Instructional illustration showing how to use epinephrine injection. The image depicts a hand holding an epinephrine auto-injector with a red tip, pushing it firmly into the thigh for 10 seconds. Arrows and text emphasize pushing the red tip hard into the thigh for proper administration.*

FDA Label Image

Figure C (Epinephrine Injection 6)

Figure C is an instructional illustration showing two hands assembling a medical device. One hand is holding a red component that is being inserted into or connected with another part held by the other hand. The arrow indicates the direction of insertion or attachment.*

FDA Label Image

Figure D (Epinephrine Injection 7)

An instructional diagram labeled Figure D showing two hands holding an epinephrine auto-injector. One hand grips the device while the other hand pulls a safety cap off by sliding it in the direction indicated by an arrow.*

* 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.