Phenylephrine Hydrochloride Injection
Product Images NDC 55150-300

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 55150-300). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us 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

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, for intravenous use. Single-dose 1 mL vial. Label indicates the product is Rx only, made in India for AuroMedics Pharma LLC, E. Windsor, NJ. Instructions include discarding unused portion and protecting from light.*
FDA Label Image

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

Package Label-principal Display Panel (10 mg per vial)
Packaging label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL for intravenous use. The carton contains 25 single-dose 1 mL vials. The label includes instructions to dilute before use, discard unused portion, and notes the product is sterile and light sensitive. Distributed by AuroMedics Pharma LLC and labeled by Auromedics.*
FDA Label Image

Phenylephrine Hydrochloride Chemical Structure (Phenylephrine Str)

Phenylephrine Hydrochloride Chemical Structure (Phenylephrine Str)
Chemical structure of phenylephrine hydrochloride, showing its molecular composition with hydroxyl groups on a benzene ring, an amine group, a methyl substituent, and the hydrochloride 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.