Bell Pharmaceuticals recalls AudoLogist's Choice Carbamide Peroxide 6.5% 0.5 fl oz (15 mL) kits due to low pH and reduced potency. Consumers should contact the manufacturer for details.
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Bell Pharmaceuticals is recalling AudoLogist's Choice carbamide peroxide products because they contain less active ingredient than expected. This could lead to ineffective treatment for users who rely on the product for medical purposes.
The product has a low pH and significantly reduced assay (about 0.6% instead of the expected 6.7%). This means the product may not work as intended for medical use, potentially leading to ineffective treatment.
People who own the recalled AudoLogist's Choice carbamide peroxide products from Bell Pharmaceuticals. Those using the product for medical purposes are most at risk.
Check for the product name 'AudoLogist's Choice', carbamide peroxide 6.5%, 0.5 fl oz (15 mL) with NDC numbers 59256-001-02 or 59256-836-34. The products were distributed by Oaktree Products Inc. in St. Louis, MO.
Reach out to Bell Pharmaceuticals for specific instructions on how to handle the recalled product.
The product has a low pH and significantly reduced assay (about 0.6% instead of the expected 6.7%), which may make it less effective for medical use.
Contact Bell Pharmaceuticals for specific instructions on how to handle the recalled product.
The recall is due to reduced potency, not a safety hazard that could cause injury. The risk is low.
We’ve drafted a message you can send Bell Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0682-2026 — Bell Pharmaceuticals Bell Pharmaceuticals Hello, I own a Bell Pharmaceuticals that is covered by recall D-0682-2026 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.
