Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Walgreens Daytime and Nighttime Cold & Flu Recalled by L. Perrigo Company Due to Labeling: Label Mix-Up - This product is being...

Date: June 5, 2017
Company: L. Perrigo Company
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact L. Perrigo Company directly.

Affected Products

Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ (355 mL) bottles connected by one paper sleeve, TOTAL 24 FL OZ (1.5 pt)(710 mL), OTC, Distributed by: Walgreen CO., 200 Wilmot Rd., Deerfield, IL 60015

Quantity: 1,998 combo packs

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 1 state: IL

Affected (1 state)Not affected

About L. Perrigo Company

L. Perrigo Company has 21 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report