Phenylephrine Hydrochloride Injection
Product Images NDC 71872-7043

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 71872-7043). 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

71872-7043-1.pdp (71872 7043 1)

Text panel for Phenylephrine Hydrochloride Injection, USP, 10 mg/mL in a 1 mL single dose vial. It includes dosage form and route (intravenous), storage instructions (20° to 25°C), dilution and usage notes, ingredient details, manufacturer and repackager information, lot and expiration placeholders, and a caution to protect from light.*

FDA Label Image

Structural Formula (Phenylephrine Hydrochloride Injection Usp Nda 1)

Chemical structure of Phenylephrine Hydrochloride, illustrating its molecular framework including a benzene ring, hydroxyl groups, and an amine hydrochloride moiety, consistent with its chemical identity as an active ingredient.*

FDA Label Image

Vial (Phenylephrine Hydrochloride Injection Usp Nda 2)

Label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL, an intravenous injection by Medical Purchasing Solutions, LLC. The label indicates a 1 mL single dose vial, with instructions to dilute before use and protect from light. Includes NDC 0641-6142-01 and a barcode.*

FDA Label Image

Layout 1 (Phenylephrine Hydrochloride Injection Usp Nda 8)

A label for Phenylephrine Hydrochloride injection, 10 mg/mL, labeled by Medical Purchasing Solutions, LLC. The label includes a GTIN barcode, serial number (SN), expiration date (EXP), and lot number (LOT) fields.*

* 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.