Epinephrine Injection
Product Images NDC 63629-8801

17 FDA label images from Bryant Ranch Prepack · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Epinephrine (NDC 63629-8801). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Structure (Image 1)

Structure (Image 1)
Chemical structure of Epinephrine showing the molecular arrangement of hydroxyl groups and amine side chain. The diagram depicts the active ingredient Epinephrine used in the injection product by Bryant Ranch Prepack.*
FDA Label Image

1 (Image 10)

1 (Image 10)
An instructional diagram showing hands removing the blue safety cap from an Epinephrine injection auto-injector. The illustration includes a yellow arrow indicating the direction to pull the cap off, demonstrating preparation for use.*
FDA Label Image

1 (Image 11)

1 (Image 11)
An instructional illustration showing a person holding an epinephrine auto-injector in their hand, positioned to inject into the outer thigh. A yellow arrow indicates the motion of pressing the device firmly against the thigh for administration.*
FDA Label Image

1 (Image 12)

1 (Image 12)
An illustration showing a hand holding an epinephrine autoinjector device positioned against the upper thigh of a person. The image demonstrates the proper intramuscular injection site for emergency use of epinephrine.*
FDA Label Image

1 (Image 13)

1 (Image 13)
An instructional image showing hands removing or twisting the blue cap on a prefilled Epinephrine injection device. A yellow arrow points downward on the cap to indicate the direction for removal or activation. The product is Epinephrine 0.15 mg/0.3 mL injection by Bryant Ranch Prepack, intended for intramuscular or subcutaneous use.*
FDA Label Image

1 (Image 14)

1 (Image 14)
Epinephrine injection auto-injector device labeled with step-by-step illustrated instructions for intramuscular or subcutaneous administration. The label includes warnings, safety release information, and handling precautions. The device is encased in a clear plastic container with a gray protective cap.*
FDA Label Image

0.3 mg Injector (Image 15)

0.3 mg Injector (Image 15)
The image shows an Epinephrine injection auto-injector by Bryant Ranch Prepack, labeled 0.15 mg per 0.3 mL for intramuscular or subcutaneous use. The device is yellow with instructional graphic labels indicating how to use it, including steps to hold, remove the safety release, press for injection, and avoiding hand placement at the needle end. The injector labels also warn to get emergency medical help immediately after use.*
FDA Label Image

0.15 mg Injector (Image 16)

0.15 mg Injector (Image 16)
Epinephrine injection auto-injector with a .15 mg/.3 mL dose by Bryant Ranch Prepack. The image shows a green and orange plastic auto-injector device with step-by-step illustrated instructions for administration by intramuscular or subcutaneous injection, including removal of the green cap, positioning, and pressing the orange end into the thigh to deliver the dose. Emergency medical help instructions are also visible.*
FDA Label Image

Ppi Image (Image 2)

Ppi Image (Image 2)
Illustration showing Bryant Ranch Prepack Epinephrine Auto-Injectors, including 0.3 mg (yellow label) with yellow cap and 0.15 mg (green label) with green cap. The image highlights features such as the yellow and green caps, blue safety release button, and orange injection tip, with both caps on and removed states for each dose.*
FDA Label Image

Ppi Ifu Image 1 (Image 3)

Ppi Ifu Image 1 (Image 3)
Instructional illustrations showing how to open the Epinephrine injection pen. The first image demonstrates removing the yellow safety cap by pulling upward. The second image shows holding the pen in one hand with the thumb on top, preparing for injection.*
FDA Label Image

Ppi Ifu Image 2 (Image 4)

Ppi Ifu Image 2 (Image 4)
An instructional illustration showing a person removing the cap from a 0.3 mL epinephrine injection device, labeled with step number 1. The image highlights the preparation step before administration of the intramuscular or subcutaneous injection.*
FDA Label Image

1 (Image 5)

1 (Image 5)
Illustration showing a person holding an Epinephrine injection autoinjector in their hand, with a yellow arrow pointing towards the person's outer thigh, indicating the injection site for intramuscular or subcutaneous administration.*
FDA Label Image

1 (Image 6)

1 (Image 6)
Illustration showing a person holding an Epinephrine injection auto-injector device. The device is orange and clear, designed for intramuscular or subcutaneous administration to deliver epinephrine, typically used in emergency situations for allergic reactions.*
FDA Label Image

1 (Image 7)

1 (Image 7)
An instructional illustration showing a hand holding an Epinephrine injection device with an orange safety cap, positioned for intramuscular or subcutaneous use. A large yellow arrow points to the left, indicating the direction for use or administration.*
FDA Label Image

1 (Image 8)

FDA Label Image

Trainer-ifu Image (Image 9)

Trainer-ifu Image (Image 9)
Diagram of an Epinephrine injection trainer showing labeled parts including a grey cap (with note not to remove until ready for use), an orange tip, and a blue safety release (also not to remove until use). The image emphasizes safety features and proper handling.*
FDA Label Image

Label (Lbl636298801)

Label (Lbl636298801)
Label for Epinephrine Injection USP 0.15 mg (Single-Dose Auto-Injectors) by Bryant Ranch Prepack. The label states the package contains two 0.15 mg epinephrine auto-injectors and one trainer, with instructions on storage and safety information. The label also includes barcode graphics and the NDC 63629-8801-1.*

* 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.