Phenylephrine Hydrochloride Injection
Product Images NDC 63323-751

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 63323-751). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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.

FDA Label Image

Structural Formula (Phe09 0007 01)

Structural Formula (Phe09 0007 01)
Chemical structure of Phenylephrine Hydrochloride showing the molecular bonds and groups including hydroxyl, amine, and aromatic ring components typical of this active ingredient.*
FDA Label Image

Fresenius Kabi Logo (Phe09 0007 02)

FDA Label Image

Package Label- Principal Display – Phenylephrine 1 mL Vial Label (Phe09 0007 03)

Package Label- Principal Display – Phenylephrine 1 mL Vial Label (Phe09 0007 03)
Label for Phenylephrine Hydrochloride Injection USP, 10 mg per mL, intended for intravenous use. The single-dose vial is 1 mL and must be diluted before use. The label includes directions to discard unused portion and protect from light. Labeler is Fresenius Kabi USA, LLC.*
FDA Label Image

Package Label- Principal Display – Phenylephrine 1 mL Vial Label (Phe09 0007 04)

Package Label- Principal Display – Phenylephrine 1 mL Vial  Label (Phe09 0007 04)
Phenylephrine Hydrochloride Injection, USP 10 mg per mL label for intravenous use. The label states to dilute before use and discard unused portions. The package contains 25 single dose vials of 1 mL each. It is labeled by Fresenius Kabi USA, LLC with storage instructions to protect from light and keep at controlled room temperature (20° to 25°C).*

* 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.