NDC 67732-414 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67732-414 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-11-14 |
| Inactivation Date | 2020-01-31 |