| NDC Code | 50580-598-02 |
|---|
| Package Description | 2 BLISTER PACK in 1 CARTON (50580-598-02) / 12 TABLET, FILM COATED in 1 BLISTER PACK |
|---|
| Product NDC | 50580-598 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Tylenol Sinus Plus Headache |
|---|
| Proprietary Name Suffix | Day |
|---|
| Non-Proprietary Name | Acetaminophen And Phenylephrine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150715 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M012 |
|---|
| Manufacturer | Johnson & Johnson Consumer Inc. |
|---|
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 325; 5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
|---|