Good Neighbor Pharmacy Earwax Removal Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Bell Pharmaceuticals is recalling Good Neighbor Pharmacy earwax removal products due to subpotent carbamide peroxide levels.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 9, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Drugs.
What Happened
Bell Pharmaceuticals, Inc. initiated a voluntary recall of Good Neighbor Pharmacy earwax removal products after testing showed the drug was subpotent, with low pH and significantly reduced assay (~0.6% vs expected ~6.7%).
Which Products Are Affected
- GOOD NEIGHBOR PHARMACY, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL)
- a) Kit - Washer Bulb Included (NDC 46122-556-05), UPC 0087701431517
- b) 1 bottle (NDC 46122-557-05), UPC 0087701431524
- Distributed by AmerisourceBergen, Conshohocken, PA
- Lot numbers: a) 1505334 (exp. 2027-04); b) 1505143, 1505151 (exp. 2027-04)
- 20,160 units distributed nationwide in the United States
- Recall number: D-0684-2026 (Class II)
What You Should Do
Consumers should discontinue use of the affected products. Contact the recalling firm or pharmacist for further guidance on returns or refunds.
Why This Matters
The affected over-the-counter earwax removal products may not deliver the expected active ingredient strength, potentially reducing effectiveness.
Source
FDA recall notice, report date 2026-07-22: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,151 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 9, 2026.
Frequently Asked Questions
Common questions about this FDA recall.