Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline Due to Failed Lozenge Specifications; Lozenges are overly thick, overly...
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 GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline directly.
Affected Products
Nicotine polacrilex lozenge, 2 mg, Original Flavor, 72 count cartons, 81 count cartons, and 108 count cartons. OTC. Labeled a. Nicorette, Distributed By: GlaxoSmithKline Consumer Healthcare, L.P., Moon Township, PA 15108. Made in Switzerland. 72 Count NDC: 0135-0510-01,108 Count NDC: 0135-0514-03, b. Nicotine Lozenge Kroger, Lozenge Kroger, Distributed by: The Kroger Company, Cincinnati, Ohio 45202, 72 Count NDC: 30142-861-01. c. Nicotine Walgreens, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015. 108 Count NDC: 0363-0208-07.
Quantity: 488,628 72 Ct Vial, 255,594 108 Ct Vial
Why Was This Recalled?
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline
GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report