Phenylephrine Hydrochloride Solution/ Drops
Product Images NDC 42702-102

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 42702-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Paragon Bioteck, Inc., 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

Chem (Chem)

Chemical structure of phenylephrine hydrochloride showing a benzene ring with hydroxyl group, an ethanolamine side chain, and an attached hydrocholoride group.*

FDA Label Image

10mlcarton (10mlcarton)

Packaging label for Phenylephrine Hydrochloride Ophthalmic Solution USP 2.5%, a topical ophthalmic solution in a 10 mL container. The label displays the Paragon BioTeck, Inc. logo and states the active ingredient strength as 25 mg/mL (2.5%). It includes usage instructions for topical ophthalmic use only and notes the solution is not for injection. Additional information includes inactive ingredients, preservative content, storage conditions, and safety warnings about the seal and dropper contamination. The label also features barcodes and distributor details from Paragon BioTeck, Inc., Bridgewater, NJ.*

FDA Label Image

5ml (5ml)

Packaging label for Phenylephrine Hydrochloride Ophthalmic Solution, USP 10%, a 5 mL solution for topical ophthalmic use only, not for injection. The label includes Paragon BioTeck, Inc. branding and states the active ingredient is phenylephrine hydrochloride at 100 mg/mL (10%). It lists inactive ingredients, preservative benzalkonium chloride 0.01%, storage instructions, and cautions. Distributed by Paragon BioTeck, Inc., product of Taiwan, with a barcode and multiple regulatory details.*

* 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.