Phenylephrine Hydrochloride Solution/ Drops
Product Images NDC 72603-530

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 72603-530). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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

Chemical Structure (0244964b Db1f 4208 B7e1 Df2244566116 01)

Chemical Structure (0244964b Db1f 4208 B7e1 Df2244566116 01)
Chemical structure of Phenylephrine Hydrochloride showing its molecular arrangement with hydroxyl groups, an amine group, and benzene ring as part of the compound's structure.*
FDA Label Image

Bottlelabel (0244964b Db1f 4208 B7e1 Df2244566116 02)

Bottlelabel (0244964b Db1f 4208 B7e1 Df2244566116 02)
Label for Phenylephrine Hydrochloride Ophthalmic Solution USP 10% strength in a 5 mL bottle. The label indicates the product is for topical application in the eye, not for injection, and is manufactured by NorthStar Rx LLC. It includes usage warnings, preservative content, storage instructions, and manufacturer information.*
FDA Label Image

Bottlecarton (0244964b Db1f 4208 B7e1 Df2244566116 03)

Bottlecarton (0244964b Db1f 4208 B7e1 Df2244566116 03)
Phenylephrine Hydrochloride Ophthalmic Solution, USP 10% (100 mg/mL) is presented in a 5 mL ophthalmic solution/drops labeled for topical eye application only, not for injection. The label includes manufacturer information, storage instructions, inactive ingredients, preservative details, dosing notes, and warnings. The product is labeled for prescription use by NorthStar Rx LLC.*

* 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.