PlainRecalls
FDA Drug Low Class III Terminated

Mucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser, Parsippany, NJ 07054-0224 UPC 363824951737 NDC 63824-207-60

Reported: September 28, 2016 Initiated: August 3, 2016 #D-1517-2016

Product Description

Mucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser, Parsippany, NJ 07054-0224 UPC 363824951737 NDC 63824-207-60

Reason for Recall

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.

Details

Recalling Firm
Reckitt Benckiser LLC
Units Affected
738 boxes
Distribution
FL, MA and NJ
Location
Parsippany, NJ

Frequently Asked Questions

What product was recalled?
Mucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser, Parsippany, NJ 07054-0224 UPC 363824951737 NDC 63824-207-60. Recalled by Reckitt Benckiser LLC. Units affected: 738 boxes.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Drug on September 28, 2016. Severity: Low. Recall number: D-1517-2016.