Olopatadine Hydrochloride Solution
Product Images NDC 68001-530

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride (NDC 68001-530). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Carton (Olopatadine Hydrochloride Ophthalmic Soln Carton Rev 03 2022)

Carton (Olopatadine Hydrochloride Ophthalmic Soln Carton Rev 03 2022)
Carton packaging label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2% (2 mg/mL) by BluePoint Laboratories. The 2.5 mL (0.085 fl oz) ophthalmic solution is labeled for eye allergy itch relief and antihistamine use. The front panel shows dosage strength, product name, directions for use once daily, and a tamper-evident notice. Drug facts and inactive ingredients are included on the side panel, along with warnings and storage instructions. The label also features a barcode and manufacturing details.*
FDA Label Image

Label (Olopatadine Hydrochloride Ophthalmic Soln Label Rev 03 2022)

Label (Olopatadine Hydrochloride Ophthalmic Soln Label Rev 03 2022)
Packaging label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2% 2.5 mL by BluePoint Laboratories. The label indicates the product is sterile, an antihistamine for eye allergy itch relief, and intended for once daily use. It includes storage instructions and tamper-evident warnings. The label also features NDC 68001-530-69 and manufacturing details by Eugia Pharma Specialities Limited.*

* 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.