Pataday Twice A Day Relief Solution
Product Images NDC 0065-4274

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pataday Twice A Day Relief (NDC 0065-4274). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alcon Laboratories, 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

Carton (Carton)

Carton (Carton)
Packaging label for Pataday Twice Daily Relief ophthalmic solution 0.1% (Olopatadine hydrochloride) by Alcon Laboratories, Inc. The label shows a 5 mL (0.17 FL OZ) sterile solution for eye allergy itch and redness relief. It highlights use for ages 2 and older with a 30-day supply. The label includes drug facts, warnings, directions, inactive ingredients, and tamper-evident instructions.*
FDA Label Image

Carton2

Carton2
Pataday Twice Daily Relief ophthalmic solution 0.1% from Alcon Laboratories, Inc. This 5 mL (0.17 fl oz) eye drop solution contains olopatadine hydrochloride as an antihistamine and redness reliever. The label highlights its use for eye allergy itch and redness relief and specifies it is for ages 2 and older with a 30-day supply. The package includes directions, warnings, inactive ingredients, and tamper-evident information.*
FDA Label Image

Label (Label)

Label (Label)
Label of Pataday Twice Daily Relief ophthalmic solution 0.1% (Olopatadine hydrochloride) by Alcon Laboratories, Inc. It is an antihistamine and redness reliever for eye allergy itch and redness relief. The label specifies a 5 mL (0.17 FL OZ) sterile solution with storage instructions and tamper-evident seal 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.