Key Takeaway

Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-022 by Reckitt Benckiser LLC was recalled on November 10, 2014. The hazard: Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch

FDA Drug Class III Terminated

Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-022

Recalled: November 10, 2014 ~155 cases (2000 pouches of 2 tablets per case) units affected D-0964-2015

Description

Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-0224 Made in England

Hazard / Reason

Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch

Class III: Product that is not likely to cause adverse health consequences.

Class III is the least severe classification. The product is unlikely to cause adverse health consequences but still violates FDA regulations.

Products Affected

Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-022

Drugs

Company Information

Reckitt Benckiser LLC

Parsippany, NJ, United States

View all 9 recalls by Reckitt Benckiser LLC →

Distribution

Nationwide

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Frequently Asked Questions

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