Phenylephrine Hydrochloride Solution
Product Images NDC 70069-591

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 70069-591). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

Image (5bc23817 Cddb 4448 Bbf3 969db4cee912 01)

Image (5bc23817 Cddb 4448 Bbf3 969db4cee912 01)
Chemical structure of Phenylephrine Hydrochloride showing the molecular arrangement including hydroxyl groups and a methylated amine, along with the hydrochloride salt component.*
FDA Label Image

Container (5bc23817 Cddb 4448 Bbf3 969db4cee912 02)

Container (5bc23817 Cddb 4448 Bbf3 969db4cee912 02)
Label for Phenylephrine Hydrochloride Injection, USP 500 mcg/5 mL (100 mcg/mL) solution for intravenous use. It is preservative-free, contains no sulfites, and comes as a 5 mL single-dose ampule. Manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. Includes instructions not to dilute and to protect from light.*
FDA Label Image

Carton (5bc23817 Cddb 4448 Bbf3 969db4cee912 03)

Carton (5bc23817 Cddb 4448 Bbf3 969db4cee912 03)
Packaging label for Phenylephrine Hydrochloride Injection, USP 500 mcg/5 mL (100 mcg/mL) sterile solution for intravenous use. The carton contains 10 single-dose 5 mL ampules. Label indicates it is preservative free, contains no sulfites, and is manufactured for Somerset Therapeutics LLC. Storage and handling instructions are also provided on the label.*

* 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.