NDC 59883-822 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59883-822 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-10-31 |
| Marketing End Date | 2013-06-13 |