NDC 51060-022 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 51060-022 |
| Marketing Category | / |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-01-01 |
| Marketing End Date | 2017-12-31 |