Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime 1000 mg/30mL
Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Pseudoephedrine HCl · SYRUP · Haleon US Holdings LLC
Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime is a syrup containing acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, pseudoephedrine hcl at 1000 mg/30mL, taken oral. Manufactured by Haleon US Holdings LLC.
Key Facts
- Brand Name
- Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime
- Generic Name
- Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Pseudoephedrine HCl
- NDC Code (Product)
0067-0114- Manufacturer
- Haleon US Holdings LLC
- Strength
- 1000 mg/30mL
- Dosage Form
- SYRUP
- Route
- ORAL
- Marketing Status
- Application #
- M012
- Marketing Start
- 06/19/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime used for?
Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime contains Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Pseudoephedrine HCl. It is a syrup taken oral. Consult your doctor for specific uses.
Is Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime a controlled substance?
Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime is not classified as a controlled substance by the DEA.
What is the generic name for Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime?
The generic name for Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime is Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Pseudoephedrine HCl. There are no other listed brand versions of Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Pseudoephedrine HCl.
What is the NDC code for Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime 1000 mg/30mL?
The NDC (National Drug Code) for Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime 1000 mg/30mL is 0067-0114, 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)