Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Mucinex Sinus-Max Day Night Recalled by Reckitt Benckiser LLC Due to Labeling: Label Error on Declared Strength; label on...
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 Reckitt Benckiser LLC directly.
Affected Products
Mucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser, Parsippany, NJ 07054-0224 UPC 363824951737 NDC 63824-207-60
Quantity: 738 boxes
Why Was This Recalled?
Labeling: Label Error on Declared Strength; label on outer carton incorrectly states Diphenhydramine 25 mg instead of 12.5 mg. Also, quantity is incorrectly stated as 30 daytime and 30 nighttime instead of 36 daytime and 24 nighttime.
Where Was This Sold?
This product was distributed to 3 states: FL, MA, NJ
About Reckitt Benckiser LLC
Reckitt Benckiser LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report