Olopatadine Hydrochloride Solution
Product Images NDC 68001-674

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olopatadine Hydrochloride (NDC 68001-674). 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

Olopatadine 0.2 Carton (Olopatadine 0.2 Carton)

Olopatadine 0.2 Carton (Olopatadine 0.2 Carton)
Packaging label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, an antihistamine eye drop with 2.5 mL (0.085 FL OZ) sterile solution. Label highlights once daily use for eye allergy itch relief, and includes instructions, drug facts, warnings, and tamper-evident packaging information. Manufactured for BluePoint Laboratories.*
FDA Label Image

Olopatadine 0.2 Label (Olopatadine 0.2 Label)

Olopatadine 0.2 Label (Olopatadine 0.2 Label)
Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, an antihistamine eye drop for eye allergy itch relief. The sterile 2.5 mL (0.085 FL OZ) bottle is for once daily use. It includes tamper-evident information, storage instructions (2°C to 25°C), and manufacturer details (SamChunDang Pharmaceutical Co., South Korea) for BluePoint Laboratories, product of Spain. NDC 68001-674.*

* 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.