Pataday Once Daily Relief Solution
Product Images NDC 0065-8150

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pataday Once Daily Relief (NDC 0065-8150). 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

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Pataday Once Daily Relief ophthalmic solution 0.2% (olopatadine hydrochloride) eye allergy itch relief solution by Alcon Laboratories, Inc. The folded carton label includes Drug Facts, usage directions, warnings, inert ingredients, and contact information. The 2.5 mL (0.085 FL OZ) bottle label indicates it is for ages 2 and older, provides a 30-day supply, and notes original prescription strength.*

FDA Label Image

Carton (Carton)

Pataday Once Daily Relief 2 mg/mL ophthalmic solution carton for eye allergy itch relief. The label shows the active ingredient olopatadine hydrochloride 0.2% antihistamine, directions for use, warnings, and the Alcon Laboratories, Inc. labeler details. The 2.5 mL bottle supply is for ages 2 and older with a 30-day supply indicated. The packaging highlights nonprescription availability and allergen relief indications.*

FDA Label Image

Label (Label)

Label for Pataday Once Daily Relief ophthalmic solution, containing olopatadine hydrochloride at 2 mg/mL (0.2% antihistamine). The sterile 2.5 mL (0.085 fl oz) solution is indicated for eye allergy itch relief. The label includes storage instructions (2°-25°C) and tamper-evident information, along with the manufacturer, Alcon Laboratories, Inc., Fort Worth, TX.*

* 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.