Phenylephrine Hydrochloride Injection
Product Images NDC 51662-1576

10 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 51662-1576). 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

Serialized Labeling (51662 1576 1 Serialized Labeling)

Serialized Labeling (51662 1576 1 Serialized Labeling)
PHENYLEPHRINE HYDROCHLORIDE injection label showing a small white sticker with a barcode and numeric codes, distributed by HF Acquisition Co., LLC in Mukilteo, WA. The label includes references to the manufacturer's package insert and the text RX ONLY, with no visible strength or dosage form details on the label itself.*
FDA Label Image

Case 1

Case 1
PHENYLEPHRINE HYDROCHLORIDE Injection 10 mg/mL in a 1 mL vial, packaging shown as a case of 25. The label includes storage instructions to protect from light and maintain temperature between 20°C to 25°C with permitted excursions. Manufactured by HF Acquisition Co LLC in Mukilteo, WA, the label also notes the product is for intravenous use and is Rx only.*
FDA Label Image

Description (Description)

Description (Description)
Chemical structure of phenylephrine hydrochloride, showing its molecular arrangement with hydroxyl groups and hydrochloride (HCl) component indicated.*
FDA Label Image

Hs (Hs)

Hs (Hs)
A data table listing product code 751101, unit of sale as NDC 63323-751-01 with a unit of 25, strength of 10 mg per mL, and individual item as NDC 63323-751-00, a 1 mL single dose vial.*
FDA Label Image
FDA Label Image

Pouch

Pouch
PHENYLEPHRINE HYDROCHLORIDE INJECTION USP 10 mg/mL in a 1 mL vial label. The label includes storage instructions, lot number, expiration date, and manufacturer information for HF Acquisition Co LLC, DBA HealthFirst. The NDC 51662-1576-2 is visible along with note of intravenous use and dilution instructions.*
FDA Label Image

Vial Label (Vial Label)

Vial Label (Vial Label)
PHENYLEPHRINE HYDROCHLORIDE Injection, USP 10 mg per mL intravenous injection label showing dosage strength, route, usage instructions to discard unused portion, single-dose vial information, and Rx only designation. The label includes NDC 63323-751-00 and appears intended for a 7.5 mL vial size, manufactured by HF Acquisition Co LLC, DBA HealthFirst.*
FDA Label Image

Vial With Label (Vial With Label)

Vial With Label (Vial With Label)
Phenylephrine Hydrochloride Injection USP 10 mg per mL in a 1 mL single-dose vial. The vial label indicates the product is for intravenous use, requires dilution before use, and unused portions must be discarded. The vial has a light blue flip-off cap.*
FDA Label Image

Vial

Vial
Label of Phenylephrine Hydrochloride Injection, USP showing 10 mg per mL strength. The label states the product is for intravenous use, in a 1 mL single dose vial, with instructions to dilute before use and to discard any unused portion. It also advises protecting the vial from light and indicates it is Rx only.*
FDA Label Image

Rfid 1

Rfid 1
A label panel including a 2D barcode, numeric codes, and text indicating distribution by HF Acquisition Co., LLC in Mukilteo, WA 98275. The label also shows the statement 'RX ONLY' and instructs to see the manufacturer's package insert. The visible data are related to product identification and traceability.*

* 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.