| NDC Code | 0363-0542-01 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0363-0542-01) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 0363-0542 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Mucus Relief Pe |
|---|
| Non-Proprietary Name | Guaifenesin, Phenylephrine Hcl |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20060415 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M012 |
|---|
| Manufacturer | Walgreen Company |
|---|
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 400; 10 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC] |
|---|