Phenylephrine Hydrochloride Injection
Product Images NDC 71872-7273

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 71872-7273). 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

Image1 (1ml Vial Label)

Image1 (1ml Vial Label)
Label for Phenylephrine HCl Injection, USP 10 mg/mL single-dose vial for intravenous use. The label instructs that the product must be diluted and unused portions discarded. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made in India. Includes barcode, lot, and expiration fields.*
FDA Label Image

71872-7273-1.pdp (71872 7273 1)

71872-7273-1.pdp (71872 7273 1)
Label for Phenylephrine HCl Injection, USP 10 mg/mL vial. The label indicates one vial per package for intravenous use, requiring dilution and protection from light. It lists ingredients including phenylephrine hydrochloride and excipients, storage instructions at 20-25°C, and manufacturer information as Caplin Steriles Limited, India, with repackaging and distribution by Medical Purchasing Solutions, Scottsdale, AZ.*
FDA Label Image

Image1 (Phenylephrine 1)

Image1 (Phenylephrine 1)
Chemical structure of PHENYLEPHRINE HYDROCHLORIDE, illustrating the molecular arrangement including a benzene ring with hydroxyl groups, an amine group, and an attached hydrochloride (HCl) molecule.*

* 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.