Phenylephrine Hydrochloride Injection
Product Images NDC 71872-7267

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 71872-7267). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

71872-7267-1.pdp (71872 7267 1)

71872-7267-1.pdp (71872 7267 1)
Label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL for intravenous use. The label states the package contains 1 vial, light sensitive, sterile, and includes storage instructions (20° to 25°C). It is repackaged and distributed by Medical Purchasing Solutions, Scottsdale, AZ. Original distribution by AuroMedics Pharma LLC, New Jersey. The vial stopper is not made with natural rubber latex.*
FDA Label Image

Package Label-principal Display Panel (10 mg per vial)

Package Label-principal Display Panel (10 mg per vial)
Label for Phenylephrine Hydrochloride Injection, USP 10 mg per mL, 1 mL single-dose vial for intravenous use. The label includes directions to dilute before use, discard unused portion, and protect from light. Manufactured in India for AuroMedics Pharma LLC, East Windsor, NJ.*
FDA Label Image

Phenylephrine Hydrochloride Chemical Structure (Phenylephrine Str)

Phenylephrine Hydrochloride Chemical Structure (Phenylephrine Str)
Chemical structure of phenylephrine hydrochloride showing a benzene ring with hydroxyl groups, a side chain with a hydroxyl and amine group, and the hydrochloride salt component.*

* 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.