Epinephrine Injection
Product Images NDC 70518-4573

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Epinephrine (NDC 70518-4573). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Label for Epinephrine Auto-Injectors 0.15 mg, subcutaneous injection, packaged in a 2-pack. Labeled with NDC 70518-4573-00 and repackaged by RemedyRepack Inc., Indiana, PA. Storage instructions note not to refrigerate and specify temperature ranges for storage. Manufacturer information for Amneal Pharma, Ahmedabad, India, is included.*
FDA Label Image

Chemical Structure (Epinephrine Injection 1)

Chemical Structure (Epinephrine Injection 1)
Chemical structure of epinephrine showing its molecular arrangement including a benzene ring with three hydroxyl groups, a side chain with a hydroxyl group, and an amine group.*
FDA Label Image

1 (Epinephrine Injection 2)

1 (Epinephrine Injection 2)
An illustrated diagram showing labeled parts of an epinephrine auto-injector 0.15 mg subcutaneous injection by RemedyRepack Inc. The components shown include a carrying case, end caps (blue), red tip labeled "needle end," viewing window for dose, and the auto-injector body with dosage labeling. The image clarifies the physical features and protective elements of the drug delivery device.*
FDA Label Image

1 (Epinephrine Injection 3)

1 (Epinephrine Injection 3)
The image shows a 0.3 mg epinephrine auto-injector with a red needle end tip and blue end caps, displayed alongside a yellow carrying case. The auto-injector features a viewing window for dose visibility and clear labeling indicating its strength. The product is designed for subcutaneous injection and is labeled by RemedyRepack Inc.*
FDA Label Image

Figure A (Epinephrine Injection 4)

Figure A (Epinephrine Injection 4)
An instructional illustration showing hands holding an epinephrine injection pen. It demonstrates the step labeled 'Twist and Pull,' indicating the twisting and pulling apart of the pen components. The action is shown with arrows and a number 1 in a circle, guiding how to prepare the injection device for use.*
FDA Label Image

Figure B (Epinephrine Injection 5)

Figure B (Epinephrine Injection 5)
An instructional diagram illustrating the removal of two blue caps from a device labeled as epinephrine injection. The image shows arrows indicating to pull off both blue caps, one from each end of a white pen-like device with a red tip.*
FDA Label Image

Figure C (Epinephrine Injection 6)

Figure C (Epinephrine Injection 6)
An instructional illustration showing step 3 in administering a subcutaneous injection. It depicts a hand pushing the red tip of an injection device firmly against the thigh, with text instructing to push the red tip hard into the thigh for 10 seconds.*
FDA Label Image

Figure D (Epinephrine Injection 7)

Figure D (Epinephrine Injection 7)
An instructional illustration showing two hands preparing an epinephrine injection. One hand holds the device with a red protective cap being pulled off in the direction indicated by a black arrow, while the other hand stabilizes the injection pen or device on the right side.*
FDA Label Image

Figure E (Epinephrine Injection 8)

Figure E (Epinephrine Injection 8)
An instructional line drawing showing two hands sliding an epinephrine injection device partially out of a box or sleeve. The device is labeled with the word "epinephrine" and includes an arrow indicating the direction to pull for removal.*

* 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.