Eye Itch Relief
Product Images NDC 62011-0232

3 FDA label images from Strategic Sourcing Services Llc · 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 Eye Itch Relief (NDC 62011-0232). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strategic Sourcing Services Llc, 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

Mck05 0005 01

Mck05 0005 01
The image shows a single white tablet blister pack marked with imprint code 'LX5'. It is a foil-type strip containing a total of 10 round tablets arranged in two columns of five. The pack is plain without additional visible markings, barcodes, or branding information.*
FDA Label Image

Mck05 0005 02

Mck05 0005 02
Label for Eye Itch Relief ophthalmic solution, containing Ketotifen Fumarate 0.035%, 5 mL (0.17 FL OZ) sterile antihistamine eye drops. Distributed by McKesson, label shows HealthMart logo. Storage instructions specify 20° to 25°C (68° to 77°F). Includes barcodes and usage warnings specific to the eye.*
FDA Label Image

Mck05 0005 03

Mck05 0005 03
The packaging label for Eye Itch Relief contains Ketotifen Fumarate Ophthalmic Solution 0.035% antihistamine eye drops in a 5 mL (0.17 FL OZ) bottle. It is for ages 3 years and older, providing up to 12 hours of relief with a 30-day supply. The product is distributed by McKesson and labeled by STRATEGIC SOURCING SERVICES LLC, with Health Mart branding. Instructions and warnings are printed on the label.*

* 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.