Clear Eyes Maximum Itchy Eye Relief Liquid
Product Images NDC 67172-999

2 FDA label images from Prestige Brands Holdings, 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 Clear Eyes Maximum Itchy Eye Relief (NDC 67172-999). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Prestige Brands Holdings, 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

Principal Display Panelclear Eyes®maximum Itchy Eye Reliefastringent/lubricant/redness Reliever Eye Drops (Clear Eyes Maximum Itchy Eye Relief 01)

Principal Display Panelclear Eyes®maximum Itchy Eye Reliefastringent/lubricant/redness Reliever Eye Drops (Clear Eyes Maximum Itchy Eye Relief 01)
Clear Eyes Maximum Itchy Eye Relief eye drops 0.5 fl oz (15 mL) packaging label. The ophthalmic liquid contains glycerin 0.25%, naphazoline hydrochloride 0.012%, and zinc sulfate 0.25%. Labeled for relief of itching, burning, watery, and red eyes. Manufactured by Prestige Brands Holdings, Inc. The carton includes product branding, ingredients, drug facts, usage directions, and tamper-evident warnings.*
FDA Label Image

Principal Display Panelclear Eyes®maximum Itchy Eye Reliefastringent/lubricant/redness Reliever Eye Drops (Clear Eyes Maximum Itchy Eye Relief 02)

Principal Display Panelclear Eyes®maximum Itchy Eye Reliefastringent/lubricant/redness Reliever Eye Drops (Clear Eyes Maximum Itchy Eye Relief 02)
Clear Eyes Maximum Itchy Eye Relief Plus eye drops in 0.2 fl oz (6 mL) liquid ophthalmic form. The front of the package highlights relief for dryness, burning, redness, and irritations with up to 12 hours of soothing comfort. The back label lists active ingredients glycerin 0.25%, naphazoline hydrochloride 0.012%, and zinc sulfate 0.25%, and provides drug facts, warnings, uses, directions, and inactive ingredients. The product is labeled sterile and distributed by Prestige Brands Holdings, Inc.*

* 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.