Phenylephrine Hydrochloride Solution/ Drops
Product Images NDC 70756-676

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 70756-676). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifestar Pharma 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

Structure (9ae3a58c 1069 4d91 B637 65d0aee9a13d 01)

Structure (9ae3a58c 1069 4d91 B637 65d0aee9a13d 01)
Chemical structure of Phenylephrine Hydrochloride, showing the molecular arrangement of atoms including hydroxyl groups, an amino group, and the hydrochloride component.*
FDA Label Image

2ml Label (9ae3a58c 1069 4d91 B637 65d0aee9a13d 02)

2ml Label (9ae3a58c 1069 4d91 B637 65d0aee9a13d 02)
Label for Phenylephrine Hydrochloride Ophthalmic Solution USP 2.5% (25 mg/mL), a 2 mL solution/drop formulation for topical eye application. The label states it is Rx only. Manufactured for Lifestar Pharma LLC, made in India, with usage and storage instructions, including not for injection and tamper-evident seal warnings, plus ingredients and preservative information.*
FDA Label Image

2ml Carton (9ae3a58c 1069 4d91 B637 65d0aee9a13d 03)

2ml Carton (9ae3a58c 1069 4d91 B637 65d0aee9a13d 03)
Carton label for Phenylephrine Hydrochloride Ophthalmic Solution USP 2.5% strength, 2 mL solution/drops for topical ocular use. The label shows the NDC 70756-629-25 and identifies Lifestar Pharma LLC as the labeler. It includes usage instructions, storage conditions, and warnings such as Rx only, not for injection, and tamper-evident seal information. Manufactured in India.*

* 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.