Epipen Injection
Product Images NDC 49502-500

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 24 technical images submitted to the FDA as part of the official labeling for Epipen (NDC 49502-500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viatris Specialty 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.

Product Images & Figures Index

FDA Label Image

Epinephrine Structural Formula (Image 01)

Epinephrine Structural Formula (Image 01)
FDA Label Image

Epipen And Epipen Jr (Image 02)

Epipen And Epipen Jr (Image 02)
This is a description of an EpiPen Auto-Injector and EpiPen Jr Autoinjector. They come with yellow and green labels respectively and are available in a carrier tube for protection. There are also instructions for how to remove them from the carrier tube. However, the text is not very clear and some of it is not readable, making it difficult to provide a complete description.*
FDA Label Image

Blue Safety Release (Image 03)

Blue Safety Release (Image 03)
The given text provides instructions for using EpiPen or EpiPen Jr. The key point mentioned is the safety release, which is provided in blue color. The text states that if the safety release is not raised, the EpiPen should not be used. But, if the blue safety release is raised, then it is safe to use the EpiPen. The text also includes two figures, one indicating that an EpiPen with a raised safety release is okay to use, while the other indicates that it should not be used and needs to be replaced.*
FDA Label Image

Instructions For Use Step 1 Figure 1 (Image 04)

Instructions For Use Step 1 Figure 1 (Image 04)
FDA Label Image

Instructions For Use Step 1 Figure 2 (Image 05)

Instructions For Use Step 1 Figure 2 (Image 05)
FDA Label Image

Instructions For Use Step 1 Figure 3 (Image 06)

Instructions For Use Step 1 Figure 3 (Image 06)
FDA Label Image

Instructions For Use Step 2 Figure 1 (Image 07)

Instructions For Use Step 2 Figure 1 (Image 07)
FDA Label Image

Instructions For Use Step 2 Figure 2 (Image 08)

Instructions For Use Step 2 Figure 2 (Image 08)
FDA Label Image

Instructions For Use Step 2 Figure 3 (Image 09)

Instructions For Use Step 2 Figure 3 (Image 09)
FDA Label Image

Instructions For Use Step 2 Figure 4 (Image 10)

Instructions For Use Step 2 Figure 4 (Image 10)
FDA Label Image

Epipen Trainer (Image 11)

Epipen Trainer (Image 11)
FDA Label Image

Practice Instructions Figure 1 (Image 12)

Practice Instructions Figure 1 (Image 12)
FDA Label Image

Practice Instructions Figure 2 (Image 13)

Practice Instructions Figure 2 (Image 13)
FDA Label Image

Practice Instructions Figure 3 (Image 14)

Practice Instructions Figure 3 (Image 14)
FDA Label Image

Practice Instructions Figure 4 (Image 15)

Practice Instructions Figure 4 (Image 15)
FDA Label Image

Comparison Trainer (Image 16)

Comparison Trainer (Image 16)
FDA Label Image

Epipen Comparison (Image 17)

Epipen Comparison (Image 17)
FDA Label Image

Epipen Jr Comparison (Image 18)

Epipen Jr Comparison (Image 18)
FDA Label Image

Epipen 0.3 mg Principal Display Panel Figure 1 (Image 19)

Epipen 0.3 mg Principal Display Panel Figure 1 (Image 19)
FDA Label Image

Epipen 0.3 mg Principal Display Panel Figure 2 (Image 20)

Epipen 0.3 mg Principal Display Panel Figure 2 (Image 20)
This appears to be an instruction manual or label for a drug delivery device. The text describes how to remove a safety release and properly administer the medication. It also includes a warning to seek emergency medical attention if necessary.*
FDA Label Image

Epipen Auto-injectors 0.3 mg Carton Label (Image 21)

Epipen Auto-injectors 0.3 mg Carton Label (Image 21)
The text appears to be a product description for EpiPen 2-Pak®, a medication used for allergic emergencies like anaphylaxis. It contains 2 single-dose auto-injectors with 0.3mg of epinephrine injection. The product also comes with a grey trainer auto-injector and should be used only under adult supervision. The carton includes two yellow EpiPen auto-injectors and the product is manufactured by Mylan. The rest of the text appears to be a combination of unidentifiable text, irrelevant numbers, and characters and hence is not useful for generating a description.*
FDA Label Image

Epipen 0.15 mg Principal Display Panel Figure 1 (Image 22)

Epipen 0.15 mg Principal Display Panel Figure 1 (Image 22)
The text describes two green EpiPen Jr auto-injectors and one grey Trainer auto-injector. It appears to be related to medical equipment typically used for emergency treatment of severe allergic reactions.*
FDA Label Image

Epipen 0.15 mg Principal Display Panel Figure 2 (Image 23)

Epipen 0.15 mg Principal Display Panel Figure 2 (Image 23)
This text instructs how to use an auto-injector. It provides steps for removing the blue safety release, swinging and pushing the orange tip firmly against the outer thigh until it clicks, and holding the injector in place for 3 seconds to deliver the drug. It also includes a warning to seek emergency medical help.*
FDA Label Image

Epipen Auto-injectors 0.15 mg Carton Label (Image 24)

Epipen Auto-injectors 0.15 mg Carton Label (Image 24)
This seems to be a product description and warning for EpiPen Jr auto-injectors containing epinephrine, used to treat anaphylaxis (allergic emergencies). Users should not put fingers or other objects over the orange tip, and the device should be used with adult supervision. The package contains two green EpiPen Jr auto-injectors and one grey trainer. The remaining text includes NDC and manufacturer information, as well as an illegible block of characters.*

* 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.