Bell Pharmaceuticals recalls QC Quality Choice carbamide peroxide 6.5% (0.5 fl oz) due to subpotent drug content. Products may have low pH and reduced effectiveness, risking inadequate treatment. Consumers should check NDC numbers and lot dates for affected items.
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Bell Pharmaceuticals is recalling QC Quality Choice carbamide peroxide products because they may have lower-than-stated effectiveness. This could lead to treatment failure if used for medical purposes like wound care. The recall affects specific lot numbers and sizes.
The product may have low pH and significantly reduced active ingredient levels (about 0.6% instead of the expected 6.7%). This could mean the product doesn't work as intended for treating wounds or skin issues. However, it does not cause immediate harm like injury or death.
People using QC Quality Choice carbamide peroxide for medical purposes, especially those with wounds or skin conditions. Those with the specific lot numbers and NDC codes listed are most at risk.
Check for the NDC numbers 63868-026-15 (with washer bulb) or 63868-027-16 (bottle), and lot numbers 1505121, 1505342, or 1505381. Products were distributed by C.D.M.A., Inc. in Novi, Michigan, and expire by April 2027.
Verify the NDC numbers and lot dates to confirm if your product is affected.
The product may have low pH and significantly reduced active ingredient levels, which could lead to treatment failure for medical uses like wound care.
Check the NDC numbers and lot dates to see if your product is affected. If it is, you may need to contact the manufacturer for further instructions.
No immediate danger is expected, but the product may not work as intended for medical purposes, so it's important to check if it's affected.
We’ve drafted a message you can send Bell Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0680-2026 — Bell Pharmaceuticals Bell Pharmaceuticals Hello, I own a Bell Pharmaceuticals that is covered by recall D-0680-2026 from Bell Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
