Class III ยท Low risk
Mucinex DM
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
National Drug Code
Is NDC 63824-0056-72 recalled?
Mucinex DM · 2 TABLET, EXTENDED RELEASE in 1 POUCH (63824-056-72)
Yes — this exact package was recalled
1 FDA recall names the code 63824-0056-72 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
- Guaifenesin and Dextromethorphan Hydrobromide
- Strength
- GUAIFENESIN 600 mg/1; DEXTROMETHORPHAN HYDROBROMIDE 30 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Reckitt Benckiser LLC
- Type
- Human OTC Drug
- Product code
- 63824-0056
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
- 63824-0008 Mucinex 3
- 63824-0014 See recall 1
- 63824-0015 Mucinex Fast-Max Cold, Flu and Sore Throat 1
- 63824-0016 See recall 1
- 63824-0019 Mucinex Fast-Max DM Max 1
- 63824-0207 See recall 1
Free recall alerts
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