Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 63868-0027-16 recalled?

Quality Choice Earwax Removal Drops · 1 BOTTLE, DISPENSING in 1 CARTON (63868-027-16) / 15 mL in 1 BOTTLE, DISPENSING

Yes — this exact package was recalled

1 FDA recall names the code 63868-0027-16 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
Liquid · Topical
Labeler
Chain Drug Marketing Association, Inc.
Type
Human OTC Drug
Product code
63868-0027

Recalls naming this package

Class II · Moderate risk

QC Quality Choice

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

Ongoing Wrong potency / content Bell Pharmaceuticals, Inc NDC 63868-026-15 D-0680-2026

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