Olopatadine Hydrochloride Solution
Product Images NDC 72036-009

2 FDA label images from Harris Teeter · 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 72036-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Harris Teeter, 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

Package Label-principal Display Panel-0.2% (2.5 mL Container) (Olopatadine Fig1)

Package Label-principal Display Panel-0.2% (2.5 mL Container) (Olopatadine Fig1)
Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, an antihistamine eye drop for allergy itch relief. The sterile solution is 2.5 mL (0.085 fl oz) in volume. The label states once daily use, storage instructions between 2° to 25°C (36° to 77°F), and tamper evidence warning. Distributed by Harris Teeter, LLC, Matthews, NC, made in India.*
FDA Label Image

Package Label-principal Display Panel-0.2% (2.5 mL Container Carton) (Olopatadine Fig2)

Package Label-principal Display Panel-0.2% (2.5 mL Container Carton) (Olopatadine Fig2)
Box label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, a 2.5 mL sterile solution by Harris Teeter. The label highlights its use for eye allergy itch relief, mentioning antihistamine properties and relief from allergens like pet dander, pollen, grass, and ragweed. It includes drug facts, directions for use, warnings, inactive ingredients, tamper-evident features, and distributor information.*

* 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.