Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0031-8760-12 recalled?

Childrens Robitussin Honey Cough and Chest Congestion DM · 1 BOTTLE in 1 CARTON (0031-8760-12) / 118 mL in 1 BOTTLE

Yes — this exact package was recalled

1 FDA recall names the code 0031-8760-12 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
dextromethorphan HBr, guaifenesin
Strength
DEXTROMETHORPHAN HYDROBROMIDE 10 mg/10mL; GUAIFENESIN 100…
Form
Solution · Oral
Labeler
Haleon US Holdings LLC
Type
Human OTC Drug
Product code
0031-8760

Recalls naming this package

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler