Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 68229-0102-01 recalled?

Clinere Ear Wax Remover

Yes — this exact package was recalled

1 FDA recall names the code 68229-0102-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

1 of these recalls is still ongoing.

Active ingredient
Carbamide Peroxide
Strength
CARBAMIDE PEROXIDE .065 g/mL
Form
Liquid · Auricular (otic)
Labeler
Quest Products
Type
Human OTC Drug
Product code
68229-0102

Recalls naming this package

Class II · Moderate risk

Clinere

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

Ongoing Wrong potency / content Bell Pharmaceuticals, Inc NDC 68229-102-01 D-0679-2026

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.