NDC 11673-722 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 11673-722 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part331 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-03-08 |
| Marketing End Date | 2018-06-30 |