| NDC Code | 55319-061-08 |
|---|
| Package Description | 236 mL in 1 BOTTLE, PLASTIC (55319-061-08) |
|---|
| Product NDC | 55319-061 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Daytime Severe Cold And Flu Relief |
|---|
| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin And Phenylephrine Hcl |
|---|
| Dosage Form | LIQUID |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20230705 |
|---|
| Marketing Category Name | OTC MONOGRAPH FINAL |
|---|
| Application Number | part341 |
|---|
| Manufacturer | FAMILY DOLLAR SERVICES INC |
|---|
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 325; 10; 200; 5 |
|---|
| Strength Unit | mg/15mL; mg/15mL; mg/15mL; mg/15mL |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
|---|