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

Is NDC 63824-0019-66 recalled?

Mucinex Fast-Max DM Max · 180 mL in 1 BOTTLE (63824-019-66)

Yes — this exact package was recalled

1 FDA recall names the code 63824-0019-66 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 hydrobromide and guaifenesin
Strength
DEXTROMETHORPHAN HYDROBROMIDE 20 mg/20mL; GUAIFENESIN 400…
Form
Solution · Oral
Labeler
Reckitt Benckiser LLC
Type
Human OTC Drug
Product code
63824-0019

Recalls naming this package

Class II · Moderate risk

Mucinex Fast Max DM Max

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.

Terminated Labeling / mix-up Reckitt Benckiser LLC NDC 63824-019-66 D-1369-2015

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