National Drug Code

Is NDC 0067-6426-01 recalled?

Q: Is NDC 0067-6426-01 recalled?

Yes - this exact package was recalled. 1 FDA recall(s) name this product; 0 still ongoing. A recall usually applies to specific lots - check the lot number on your package and ask your pharmacist.

Theraflu Multi-Symptom Severe Cold

Yes — this exact package was recalled

1 FDA recall names the code 0067-6426-01 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: ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl
Strength: ACETAMINOPHEN 500 mg/237mL; DEXTROMETHORPHAN HYDROBROMIDE…
Form: Powder, for Solution · Oral
Labeler: Haleon US Holdings LLC
Type: Human OTC Drug
Product code: 0067-6426

Recalls naming this package

Jun 18, 2013 Class II · Moderate risk

Theraflu Multi-Symptom Severe Cold

Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

Terminated Particulate / foreign matter Novartis Consumer Health NDC 0067-6426-06 D-752-2014

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

0067-2081 See recall 2
0067-6438 See recall 2
0067-0343 See recall 1
0067-0376 See recall 1
0067-2062 See recall 1
0067-2082 See recall 1

Yes — this exact package was recalled

Recalls naming this package

Theraflu Multi-Symptom Severe Cold

Other recalled products from this labeler

Know the day your medication is recalled