NDC 63029-402 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63029-402 |
| Marketing Category | / |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-09-01 |
| Inactivation Date | 2019-10-29 |