Chemical Structure (0244964b Db1f 4208 B7e1 Df2244566116 01)
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.
Bottlelabel (0244964b Db1f 4208 B7e1 Df2244566116 02)
This is a description of an ophthalmic solution containing Phenylephrine Hydrochloride, intended for topical application and not for injection. The solution is meant for use in the eye and each milliliter contains 100 mg of Phenylephrine Hydrochloride USP. It also contains Benzalkonium Chloride as a preservative. The recommended storage conditions are between 20°C to 25°C (68°F to 77°F) at controlled room temperature, protected from light and excessive heat. The solution should not be used if it is discolored or contains a precipitate. It is important to keep the container tightly closed and not to use if the tamper-evident seal is broken or missing. It is noted that the bottle is filled to half capacity for proper drop control. The solution can be used until the expiration date after opening. The product is manufactured by Northstar Rx LLC based in Memphis, TN.*
Bottlecarton (0244964b Db1f 4208 B7e1 Df2244566116 03)
This is a detailed label of Phenylephrine Hydrochloride Ophthalmic Solution, USP manufactured in India by Mankind Pharma Limited. The solution is intended for topical application in the eye and should not be injected. It contains 100 mg of Phenylephrine Hydrochloride USP in each mL, with added ingredients like sodium phosphate and benzalkonium chloride as a preservative. The proper storage conditions are specified, and usage instructions are available in the package insert. The label also includes a caution about not using the solution if it has changed color or contains a precipitate. The product is packaged in a bottle with proper drop control and the company information for Northstar Rx LLC in Memphis, TN is provided.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
