Theraflu Severe Cold Relief Daytime Berry Burst 650 mg/1
Acetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride · POWDER · Haleon US Holdings LLC
Theraflu Severe Cold Relief Daytime Berry Burst is a powder containing acetaminophen, dextromethorphan hbr, phenylephrine hydrochloride at 650 mg/1, taken oral. Manufactured by Haleon US Holdings LLC.
Key Facts
- Brand Name
- Theraflu Severe Cold Relief Daytime Berry Burst
- Generic Name
- Acetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride
- NDC Code (Product)
0067-6800- Manufacturer
- Haleon US Holdings LLC
- Strength
- 650 mg/1
- Dosage Form
- POWDER
- Route
- ORAL
- Marketing Status
- Application #
- M012
- Marketing Start
- 01/20/2022
Recall History
No Recall HistoryFrequently Asked Questions
What is Theraflu Severe Cold Relief Daytime Berry Burst used for?
Theraflu Severe Cold Relief Daytime Berry Burst contains Acetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride. It is a powder taken oral. Consult your doctor for specific uses.
Is Theraflu Severe Cold Relief Daytime Berry Burst a controlled substance?
Theraflu Severe Cold Relief Daytime Berry Burst is not classified as a controlled substance by the DEA.
What is the generic name for Theraflu Severe Cold Relief Daytime Berry Burst?
The generic name for Theraflu Severe Cold Relief Daytime Berry Burst is Acetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride. There are no other listed brand versions of Acetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride.
What is the NDC code for Theraflu Severe Cold Relief Daytime Berry Burst 650 mg/1?
The NDC (National Drug Code) for Theraflu Severe Cold Relief Daytime Berry Burst 650 mg/1 is 0067-6800, listed by Haleon US Holdings LLC.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)