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Class II · ModerateActive recall

Clinere Ear Wax Remover

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

Does this affect you?
Check your lot numberLot: a) 1504241, exp 2027-03; b) 1504291, 1504301, exp 2027-03.
Where it was soldU.S Nationwide
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

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

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 byQuest Products
Brand nameCLINERE EAR WAX REMOVER
Generic nameCARBAMIDE PEROXIDE
Active ingredient(s)CARBAMIDE PEROXIDE
Distributed by / forBell Pharmaceuticals, Inc
NDC68229-102-01
Show the full FDA record
Full product labelClinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%, 0.5 fl. oz. (15 mL); b) 1 bottle of Clinere Carbamide Peroxide (0,50 fl. oz. (15 mL), Dist. by: Quest Products LLC, Pleasant Prairie, WI 53158, NDC 68229-102-01.
Recalling firmBell Pharmaceuticals, Inc
DistributionU.S Nationwide
Quantity29, 474 units
Recall initiated2026-06-25
Report date2026-07-22
Recall completed—
Recall numberD-0679-2026
ClassificationClass II
FDA statusOngoing
Origin on fileBelle Plaine MN United States

Related

Recent drug recallsCheck another medication

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.