Adrenalin (epinephrine) Injection
Product Images NDC 51662-1290

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Adrenalin (epinephrine) (NDC 51662-1290). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Vial Label (1007670 42023 159 25 Adrenalin Sourse Vial Label (1))

Label for Epinephrine Convenience Kit (Adrenalin) showing epinephrine injection, USP, 1 mg/mL strength. Indicated for intramuscular and subcutaneous use, not for ophthalmic use, in a 1 mL single-dose vial. Manufactured by HF Acquisition Co LLC, DBA HealthFirst. Includes NDC 42023-159-25 and space for lot and expiration information.*

FDA Label Image

51662-1290-1 Serialized Vial Labeling (51662 1290 1 Adrenalin Serialized Vial Labeling)

The image shows a single-dose vial of Adrenalin (epinephrine injection, USP) with a strength of 1 mg/mL. The vial has a purple cap and a white label indicating its use for intramuscular and subcutaneous administration, with a warning that it is not for ophthalmic use. A barcode label is also visible, displaying distribution information from HF Acquisition Co., LLC in Mukilteo, WA.*

FDA Label Image

Alcohol Prep Pad (BACK)

Drug Facts panel for a topical product listing its uses for removal of oils and residue from skin, directions for application avoiding eyes and large skin areas, warnings against use in eyes, and flammability precautions. Ingredients include isopropyl alcohol and water. Manufacturer info and lot number are visible.*

FDA Label Image

Alcohol Prep Pad (FRONT)

Packaging label of a rectangular alcohol prep pad from Medline. The label states it is a medium size alcohol prep pad containing 70% isopropyl alcohol, sterile in an unopened package, single use, and not made with natural rubber latex.*

FDA Label Image

Epi Convenience Kit Labeling (Epi Convenience Kit Labeling)

Label of Epinephrine Convenience Kit by HF Acquisition Co LLC DBA HealthFirst. The kit contains 1 mg/mL Epinephrine Injection (Adrenalin) vial, EpiRite syringes, 20G needles, and alcohol prep pads. The label states Rx only, storage between 20° to 25°C, and notes that the product is not made with natural rubber latex. The label includes North American Rescue contact info.*

FDA Label Image

Epirite Syringe Labeling (Epirite Syringe Labeling)

Packaging label of Epirite Syringe sterile single-use syringes shown in their sealed wrapping. Each syringe packet includes details such as lot number, expiration date, and manufacturer information. The syringes are part of the Epinephrine Convenience Kit by HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Hypodermic Needle Labeling (Hypodermic Needle Labeling)

Packaging labels for two sterile hypodermic needles, both marked 19G x 1". The labels show sterile status and batch information, but no brand or drug details. These needles are likely components within the Epinephrine Convenience Kit for intramuscular or subcutaneous use by HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Serialization Example Labeling (Serialization Example Labeling)

Epinephrine Convenience Kit label showing barcode data. The label includes references to the Epinephrine Manufacturer's Package Insert and states that the kit is manufactured and packaged by HF Acquisition Co., LLC in Mukilteo, WA 98275. The label also includes regulatory coding and "RX ONLY" designation.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of epinephrine, showing its molecular framework including a benzene ring with three hydroxyl groups and an attached side chain with amine and hydroxyl functional groups.*

* 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.