Epinephrine
Product Images NDC 51662-1221

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Epinephrine (NDC 51662-1221). 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

00351662122129 Epinephrine Pouch Label

Label for EPINEPHRINE Injection USP 1 mg/10 mL (0.1 mg/mL) 10 mL syringe by HF Acquisition Co LLC, DBA HealthFirst. The label includes NDC 51662-1221-2, lot number 12345, and expiration date 2025-01-01. Additional warnings and storage instructions are partially visible.*

FDA Label Image

00351662122136 Epinephrine Rfid Label

A label showing serialized data and distribution information for EPINEPHRINE by HF Acquisition Co LLC, DBA HealthFirst. The label includes bar code data with GS1 element strings, lot number, expiration date (January 1, 2025), and states "See manufacturer's package insert." It also mentions the distributor's address in Mukilteo, WA 98275, and "RX ONLY."*

FDA Label Image

00351662122136 Epinephrine Case Label (1)

Label for EPINEPHRINE INJECTION, USP 1mg/10mL (0.1mg/mL) 10mL syringe, box of 50, manufactured by HF Acquisition Co LLC. The label shows NDC 51662-1221-3, lot number 12345, and expiry date 2025-01-01. It includes warnings and storage instructions along with a QR code and manufacturer address in Mukilteo, WA.*

FDA Label Image

Serialized Box (51662 1221 1 Epinephrine Injection 10 Serialized Label)

EPINEPHRINE Injection USP 1 mg/1 mL (10 mg/mL) single-dose unit in carton packaging labeled by HF Acquisition Co LLC, DBA HealthFirst. The carton includes storage instructions, warnings about sulfites, and directions to discard unused portions. It is protected from light until use and stored at controlled room temperature (20 to 25°C).*

FDA Label Image

How Supplied Logo (How Supplied Logo)

FDA Label Image

How Supplied Tabel (How Supplied)

A table displaying unit of sale information for Epinephrine, including total strength and volume (1 mg/10 mL or 0.1 mg/mL concentration), with NDC codes for bundles of 10 and individual 10 mL single-dose glass syringes (Abboject and Lifeshield Abboject). Syringe specifications with gauge and length are included.*

FDA Label Image

Logo (Logo)

FDA Label Image

Structure (Structure)

Chemical structure diagram of epinephrine showing its molecular components including a benzene ring with two hydroxyl groups and side chains with hydroxyl and methylamine groups.*

FDA Label Image

Carton (Updated 0409 4921 20 Epinephrine Syr Box Label)

Packaging label for EPINEPHRINE Injection, USP 1 mg/10 mL (0.1 mg/mL) by HF Acquisition Co LLC, DBA HealthFirst. The label includes dosage form as a glass ABOJECT unit of use syringe with a male luer lock adapter and 20-gauge protected needle. It contains cautionary instructions for handling the liquid vial and aseptic technique for using the syringe. The label also includes warnings such as protection from light and sulfite content. The label displays the NDC 0409-4921-20 and features Lifeshield branding along with Hospira manufacturer information.*

FDA Label Image

Syringe (Updated Syringe)

Label for EPINEPHRINE Injection, USP 1 mg/10 mL (0.1 mg/mL) single-dose vial by HF Acquisition Co LLC, DBA HealthFirst. Includes measurement markings up to 10 mL. Label states sterile, nonpyrogenic, pH 3.3, for intravenous use, and lists manufacturer as Hospira, Inc., Lake Forest, IL. Contains barcode and NDC 0409-4921-20.*

* 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.