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

National Drug Code

Is NDC 51316-0822-00 recalled?

CVS Health Earwax Removal Drops Earwax Removal Aid · 1 BOTTLE in 1 BOX (51316-822-00) / 15 mL in 1 BOTTLE

Yes — this exact package was recalled

1 FDA recall names the code 51316-0822-00 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 65 mg/mL
Form
Solution/ Drops · Topical
Labeler
CVS Pharmacy, Inc.
Type
Human OTC Drug
Product code
51316-0822

Recalls naming this package

Class II · Moderate risk

CVS Health

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

Ongoing Wrong potency / content Bell Pharmaceuticals, Inc NDC 51316-822-00 D-0678-2026

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.

Other recalled products from this labeler