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FDAJanuary 8, 2016drug

Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan HBr 5 mg/5 mL), packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold under the following: a) Sunmark, Children's Mucus Relief Cough, Guaifenesin 100 mg/Expectorant, Dextromethorphan HBr 5 mg/Cough S...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.

What to do

FDA enforcement status: Terminated

Brands named

perrigo company plcperrigoperrigo company

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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