New Vision Pharmaceuticals recalls 8-vial cold and flu relief products due to subpotent drug content. This means the medication may not be as effective as intended. Consumers should contact the manufacturer for details.
Subpotent Drug
New Vision Pharmaceuticals is recalling daytime cold and flu relief vials because they contain less active ingredient than labeled. This could mean the medicine isn't as effective as it should be, but it doesn't pose a safety risk.
The product contains a subpotent drug, meaning it has less active ingredient than stated. This could lead to the medication being less effective than intended, but it does not cause harm or injury.
People who bought the Daytime Severe Cold & Flu Relief 8-vial products from CVS Pharmacy in the US. Those most at risk are individuals using the medication for cold or flu symptoms.
Check for the product name 'Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials' with NDC 69842-495-16 or UPC 050428640579. The product was distributed by CVS Pharmacy and expired June 8, 2023.
Reach out to New Vision Pharmaceuticals for specific instructions on how to handle the recalled product.
Yes, the product is safe but may not be as effective as labeled due to subpotent drug content.
Contact New Vision Pharmaceuticals for specific instructions on handling the recalled product.
The product was distributed by CVS Pharmacy starting in 2021 with an expiration date of June 8, 2023.
We’ve drafted a message you can send New Vision Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0852-2021 — New Vision Pharmaceuticals New Vision Pharmaceuticals Hello, I own a New Vision Pharmaceuticals that is covered by recall D-0852-2021 from New Vision 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
