Olopatadine Hydrochloride Ophthalmic Solution Solution/ Drops
Product Images NDC 68083-477

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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 Ophthalmic Solution (NDC 68083-477). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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-bottle-label (Olopatadine Bottle Label)

Olopatadine-bottle-label (Olopatadine Bottle Label)
Olopatadine Hydrochloride Ophthalmic Solution USP 0.1% label by Gland Pharma Limited. The label states each mL contains 0.1% olopatadine (equivalent to 0.111% olopatadine hydrochloride) and the solution is sterile. It is a 5 mL eye drop solution for antihistamine and redness relief, with storage instructions and tamper-evident warnings.*
FDA Label Image

Olopatadine-carton-label (Olopatadine Carton Label)

Olopatadine-carton-label (Olopatadine Carton Label)
Packaging label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.1%, 5 mL sterile drops by Gland Pharma Limited. The label highlights antiallergic and redness relief properties for eye allergy itch and redness. Directions specify use twice daily for adults and children 2 years and older. Includes active ingredient concentration and safety warnings.*

* 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.