US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 16, 2020 (6 years ago)

Childrens Robitussin Honey Cough and Chest Congestion DM, dextromethorphan (cough…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

What was recalled

Childrens Robitussin Honey Cough and Chest Congestion DM, dextromethorphan (cough suppressant), guaifenesin (expectorant), 4 FL OZ. bottle (118 mL), Distributed by: Pfizer, Madison, NJ 07940 USA, UPC: 50300318760128, NDC: 0031-8760-12.

Recalling firm
Glaxosmithkline Consumer Healthcare Holdings
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1361-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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