Reported Sep 2, 2015 · Terminated

Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Time Cold & Flu Two - 6 fl oz (180 mL) bottles Total -12 fl oz…

Reckitt Benckiser LLC

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Reckitt Benckiser LLC · 399 Interpace Pkwy · Parsippany, NJ · 07054-1133

Is this the product you have?

  • Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Time Cold & Flu Two - 6 fl oz (180 mL) bottles Total -12 fl oz (360 mL), For Age 12+, Dist
  • By
    • Reckitt Benckiser Parsippany
    • NJ 07054-0224 Made in India
    • NDC 63824-526-22
Lot codes and dates
    • WO00726864
    • 6/30/2016
    • WO00737979
    • 1/31/2017
    • WO00740405
    • 1/31/2017
    • WO00706571
    • 7/31/2016
    • WO00707442
    • 7/31/2016
    • WO00707443
    • 7/31/2016
    • WO00707444
    • 7/31/2016
    • WO00707822
    • 7/31/2016
    • WO00709953
    • 7/31/2016
    • WO00709955
    • 6/30/2016
    • WO00720780
    • 7/31/2016
    • WO00721052
    • 7/31/2016
    • WO00721170
    • 7/31/2016
    • WO00721171
    • 7/31/2016
    • WO00726865
    • 7/31/2016
    • WO00728864
    • 7/31/2016
    • WO00728865
    • 12/31/2016
    • WO00728866
    • 12/31/2016
    • WO00730003
    • 12/31/2016
    • WO00730004
    • 12/31/2016
    • WO00735142
    • 12/31/2016
    • WO00736753
    • 12/31/2016
    • WO00737477
    • 1/31/2017
    • WO00738556
    • 12/31/2016
    • WO00739050
    • 12/31/2016
    • WO00740406
    • 1/31/2017
Amount recalled
561,390 Bottles

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Mar 9, 2018 · Data as of Sep 19, 7:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.