Recall of Nighttime Sleep-Aid tablets due to incorrect labeling as doxylamine succinate HCl when product is actually doxylamine succinate. No remedy provided.
Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as doxylamine succinate HCl, however the product is doxylamine succinate.
LNK International recalls Nighttime Sleep-Aid tablets that are incorrectly labeled as doxylamine succinate HCl. The product is actually doxylamine succinate, which may cause confusion with a different medication. This recall does not pose a safety risk but requires consumers to check their labels.
The product is labeled as doxylamine succinate HCl but is actually doxylamine succinate. This labeling error could lead to confusion with a different medication, potentially causing incorrect use or medication errors.
Anyone who owns or uses Nighttime Sleep-Aid tablets distributed by CVS. People most at risk are those who may have taken the product without realizing the labeling error.
Check for Nighttime Sleep-Aid tablets with the product code P121512 through P129536, distributed by CVS. The product was sold between 2023 and 2025 with specific expiration dates.
Verify the product label to confirm it is doxylamine succinate, not doxylamine succinate HCl.
No, the recall is due to labeling error, not a safety hazard. The product is safe but may be confused with a different medication.
Check the label to confirm it is doxylamine succinate, not doxylamine succinate HCl. No action is needed if the label matches.
Look for Nighttime Sleep-Aid tablets with product codes P121512 through P129536, distributed by CVS with specific expiration dates.
We’ve drafted a message you can send LNK International to request your refund or repair — edit it as you like.
Subject: Recall D-1472-2022 — LNK International LNK International Hello, I own a LNK International that is covered by recall D-1472-2022 from LNK International. 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.
