Pharma Nobis recalls 6.5% carbamide peroxide earwax drops due to potential active ingredient degradation before expiry. Consumers should check product lots and contact CVS for details.
CGMP Deviations: active ingredient may be subpotent before the labeled expiry due to degradation.
Pharma Nobis is recalling earwax drops that may have less active ingredient than labeled due to degradation. This could reduce effectiveness but does not pose a direct health risk to users.
The active ingredient (carbamide peroxide) may degrade over time, making the product less effective than labeled. This could lead to reduced earwax removal results but does not cause injury or illness.
People who purchased the earwax drops from CVS Pharmacy with the listed lot numbers and expiration dates. Those using the product for earwax removal are most at risk if they need the drops to be effective.
Check the product label for the lot numbers: A70293-A70295 (exp. 12/2023), A70746-A70749 (exp. 01/2024), or A73051-A73052 (exp. 05/2024). The product is sold at CVS Pharmacy stores.
Look for lot numbers on the bottle: A70293-A70295 (exp. 12/2023), A70746-A70749 (exp. 01/2024), or A73051-A73052 (exp. 05/2024).
Reach out to CVS Pharmacy for further assistance with the recall.
No, the recall is for reduced effectiveness due to potential ingredient degradation, not a safety hazard.
Check the lot numbers on the bottle: A70293-A70295 (exp. 12/2023), A70746-A70749 (exp. 01/2024), or A73051-A73052 (exp. 05/2024).
The recall does not require discarding the product; contact CVS Pharmacy for guidance.
We’ve drafted a message you can send Pharma Nobis to request your refund or repair — edit it as you like.
Subject: Recall D-0537-2023 — Pharma Nobis Pharma Nobis Hello, I own a Pharma Nobis that is covered by recall D-0537-2023 from Pharma Nobis. 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.
