NDC 30142-224 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 30142-224 |
| Marketing Category | / |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part335 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-06-03 |
| Marketing End Date | 2017-06-01 |