FDA recall record

Reckitt Benckiser Mucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser recall — FDA D-1517-2016

Labeling: Label Error on Declared Strength; label on outer carton incorrectly states Diphenhydramine 25 mg instead of 12.5 mg. Also, quantity is…

Class IIIclassification
D-1517-2016official record ID
Sep 28, 2016report date

Recall record at a glance

Official recordD-1517-2016
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmReckitt Benckiser LLC
Report dateSep 28, 2016
Recall initiation dateAug 3, 2016
Quantity738 boxes
LocationParsippany, NJ, United States

Official product description

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

Why the product was 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.

Distribution information

FL, MA and NJ

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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