CVS recalls Multi Action Relief Drops due to non-sterility risk. Affected bottles contain polyvinyl alcohol and tetrahydrozoline. Consumers should check NDC 76168-706-15 and lot numbers.
Non-Sterility
CVS is recalling Multi Action Relief Drops because they may not be sterile. This could lead to infections if used. The recall covers all bottles with the specific NDC number and lot numbers.
The product may not be sterile, which could lead to infections if used. This is a non-sterility hazard, meaning the product might not meet safety standards for medical use.
People who own or use CVS Multi Action Relief Drops with NDC 76168-706-15 are affected. Those with the specific bottle size and lot numbers are most at risk.
Check for the NDC code 76168-706-15 on the bottle. The product is packaged in 0.5 fl oz (15mL) bottles. All lots are affected.
Look for the NDC code 76168-706-15 on the bottle label.
The recall states the product may not be sterile, so it could pose an infection risk. Do not use until you confirm it's safe.
Check for the NDC code 76168-706-15 on the bottle. The product is packaged in 0.5 fl oz (15mL) bottles.
The recall does not specify a remedy, so you should check with CVS Pharmacy Inc. for further instructions.
We’ve drafted a message you can send CVS to request your refund or repair — edit it as you like.
Subject: Recall D-0296-2024 — CVS CVS Hello, I own a CVS that is covered by recall D-0296-2024 from CVS. 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.
