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

2 FDA label images from Gland Pharma Limited · 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 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.

Product Images & Figures Index

FDA Label Image

Olopatadine-spl-bottle (Olopatadine Spl Bottle)

Olopatadine-spl-bottle (Olopatadine Spl Bottle)
Label for Olopatadine Hydrochloride Ophthalmic Solution, USP 0.1%, a sterile solution for eye use, 5 mL (0.17 fl oz) bottle. It identifies the product as an antihistamine and redness reliever for eye allergy itch and redness, to be used twice daily. Manufactured by Gland Pharma Limited in Hyderabad, India. Includes storage instructions, tamper evidence warning, lot number, expiration date fields, and a barcode.*
FDA Label Image

Olopatadine-spl-carton (Olopatadine Spl Carton)

Olopatadine-spl-carton (Olopatadine Spl Carton)
Packaging label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.1%, a sterile eye drop solution labeled as an antihistamine and redness reliever. The 5 mL (0.17 fl oz) bottle is indicated for eye allergy itch and redness relief with twice-daily use. The label includes drug facts, usage instructions for adults and children 2 years and older, warnings, inactive ingredients, barcode, and manufacturer information from Gland Pharma 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.