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Class II · ModerateActive recall

Clear Eyes Maximum Itchy Eye Relief

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot 2552A, Exp 09/30/2027
Where it was soldNationwide in the USA.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Lack of assurance of sterility. The recall is due to potential contamination

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byPrestige Brands Holdings, Inc.
Brand nameCLEAR EYES MAXIMUM ITCHY EYE RELIEF
Generic nameGLYCERIN AND NAPHAZOLINE HYDROCHLORIDE AND ZINC SULFATE
Active ingredient(s)GLYCERIN, NAPHAZOLINE HYDROCHLORIDE, ZINC SULFATE
Distributed by / forPrestige Brands Holdings
NDC67172-999-01
Show the full FDA record
Full product labelCLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3
Recalling firmPrestige Brands Holdings
DistributionNationwide in the USA.
Quantity39,060 15mL-bottles
Recall initiated2026-07-29
Report date2026-08-19
Recall completed
Recall numberD-0766-2026
ClassificationClass II
FDA statusOngoing
Origin on fileTarrytown NY United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.