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

Is NDC 70677-1154-01 recalled?

Foster and Thrive Earwax Removal Drops · 1 BOTTLE in 1 BOX (70677-1154-1) / 15 mL in 1 BOTTLE

Yes — this exact package was recalled

1 FDA recall names the code 70677-1154-01 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 65 mg/mL
Form
Solution/ Drops · Topical
Labeler
Mckesson Corp. Via Strategic Sourcing Services
Type
Human OTC Drug
Product code
70677-1154

Recalls naming this package

Class II · Moderate risk

Foster & Thrive

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

Ongoing Wrong potency / content Bell Pharmaceuticals, Inc NDC 70677-1154-01 D-0686-2026

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