| Product NDC: | 42192-521 |
| Proprietary Name: | Pyrilamine-Phenylephrine |
| Non Proprietary Name: | Pyrilamine Maleate and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 5; 16 mg/5mL; mg/5mL & nbsp; Pyrilamine Maleate and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42192-521 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120822 |
| Package NDC: | 42192-521-16 |
| Package Description: | 473 mL in 1 BOTTLE (42192-521-16) |
| NDC Code | 42192-521-16 |
| Proprietary Name | Pyrilamine-Phenylephrine |
| Package Description | 473 mL in 1 BOTTLE (42192-521-16) |
| Product NDC | 42192-521 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pyrilamine Maleate and Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120822 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE MALEATE |
| Strength Number | 5; 16 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |