Olopatadine Hydrochloride Solution/ Drops
Product Images NDC 62332-709

2 FDA label images from Alembic Pharmaceuticals Inc. · 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 62332-709). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Inc., 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-carton (Olopatadine Carton)

Olopatadine-carton (Olopatadine Carton)
Olopatadine Hydrochloride 0.1% Ophthalmic Solution, USP is an antihistamine and redness reliever in a 5 mL (0.17 FL OZ) sterile eye drop solution. The label highlights its use for eye allergy itch and redness relief, suitable for ages 2 and older, with a 30-day supply. It is manufactured by Alembic Pharmaceuticals Inc., with NDC 62332-709-05.*
FDA Label Image

Olopatadine-container (Olopatadine Container)

Olopatadine-container (Olopatadine Container)
Olopatadine Hydrochloride Ophthalmic Solution USP 0.1% (1 mg/mL) in a 5 mL sterile bottle carton, labeled as an antihistamine and redness reliever for eye allergy itch and redness relief, to be used twice daily. Manufactured for Alembic Pharmaceuticals Inc., with storage instructions and tamper-evident warning visible.*

* 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.