Walgreens Daytime Nighttime Cold Flu Combo Pack Recall: Incorrect Product Sleeve
Walgreens Daytime and Nighttime Cold & Flu combo pack recalled due to incorrect product sleeve labeling. This mix-up means the product contains Day-Night Cough Liquid instead of Cold & Flu.
Lower-risk recall
Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the batch contains Day-Night Cough Liquid.
Contact the company
What happened, in plain English
Walgreens Daytime and Nighttime Cold &: Flu combo packs are being recalled because the product sleeve labels them as Day-Night Cold & Flu when they actually contain Day-Night Cough Liquid. This mix-up means customers might be using the wrong product for their symptoms. Read more at govinfonow.com/recall/41584-walgreens-daytime-nighttime-cold-flu-combo-pack-recall-incorrect-product.
Source Summary by GovInfoNow · govinfonow.com/recall/41584-walgreens-daytime-nighttime-cold-flu-combo-pack-recall-incorrect-product · Updated October 8, 2026 · FDA enforcement record: FDA #D-0925-2017
Cite this page
“Walgreens Daytime Nighttime Cold Flu Combo Pack Recall: Incorrect Product Sleeve.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41584-walgreens-daytime-nighttime-cold-flu-combo-pack-recall-incorrect-product. Based on FDA recall #D-0925-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0925-2017%22&limit=1).
Why it’s dangerous
The product sleeve incorrectly identifies the product as Day-Night Cold & Flu, but the actual contents are Day-Night Cough Liquid. This mix-up could lead to customers taking cough medicine instead of cold/flu medicine, which may not address their symptoms properly.
Who’s affected
Anyone who purchased the Walgreens combo pack of Daytime and Nighttime Cold & Flu bottles with the incorrect sleeve label. People using cough medicine instead of cold/flu medicine are most at risk.
How to tell if you have this one
Look for Walgreens Daytime and Nighttime Cold & Flu combo packs with two plastic 12FL OZ bottles connected by a paper sleeve. The product contains Day-Night Cough Liquid instead of Cold & Flu.
- Brand
L. Perrigo Company- Category
Drug
What to do — step by step
Check Product Label
Verify the product sleeve label matches the actual contents (Day-Night Cough Liquid) to ensure you have the correct product.
Where it went and when
Where it was distributed
Distributed in Illinois.
FDA distribution: “IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest drug recalls
Keep exploring
Where this comes from
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.
- Official source: FDA Recall #D-0925-2017 (June 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0925-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.