NDC 42002-214 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42002-214 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part349 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-06-03 |
| Marketing End Date | 2018-03-01 |