| NDC Code | 0067-8205-01 |
|---|
| Package Description | 245.5 mL in 1 BOTTLE (0067-8205-01) |
|---|
| Product NDC | 0067-8205 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Theraflu Flu Relief Max Strength |
|---|
| Proprietary Name Suffix | Nighttime |
|---|
| Non-Proprietary Name | Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hbr |
|---|
| Dosage Form | SYRUP |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220627 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M012 |
|---|
| Manufacturer | Haleon US Holdings LLC |
|---|
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE |
|---|
| Strength | 1000; 4; 30 |
|---|
| Strength Unit | mg/30mL; mg/30mL; mg/30mL |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
|---|