| NDC Code | 69423-922-12 |
|---|
| Package Description | 354 mL in 1 BOTTLE, PLASTIC (69423-922-12) |
|---|
| Product NDC | 69423-922 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Vicks Dayquil |
|---|
| Proprietary Name Suffix | Cough Dm Plus Congestion |
|---|
| Non-Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin And Phenylephrine Hydrochloride |
|---|
| Dosage Form | LIQUID |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20210101 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M012 |
|---|
| Manufacturer | The Procter & Gamble Manufacturing Company |
|---|
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 10; 200; 5 |
|---|
| Strength Unit | 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] |
|---|