NDC 51239-0912 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 51239-0912 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-03-01 |
| Inactivation Date | 2019-10-21 |