Olopatadine Hydrochloride Solution
Product Images NDC 72036-008

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 72036-008). 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-0.1% (5 mL Container) (Olopatadine Fig1)

Package Label-principal Display Panel-0.1% (5 mL Container) (Olopatadine Fig1)
Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.1% by Harris Teeter. The sterile eye solution relieves eye allergy itch and redness. Package contains 5 mL (0.17 FL OZ). Instructions indicate twice daily use and storage at 4° to 25°C. Distributed by Harris Teeter, LLC, Matthews, NC 28105. Made in India.*
FDA Label Image

Package Label-principal Display Panel-0.1% (5 mL Container Carton) (Olopatadine Fig2)

Package Label-principal Display Panel-0.1% (5 mL Container Carton) (Olopatadine Fig2)
The packaging label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.1%, an eye allergy itch and redness relief solution. The 5 mL (0.17 fl oz) eye drop container is sterile and labeled for twice daily use. It is distributed by Harris Teeter, with the label also stating the product is made in India. The label highlights relief from allergens including pet dander, pollen, grass, and ragweed, and includes tamper-evident instructions and directions for use.*

* 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.