NDC 69512-001 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69512-001 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-01-21 |
| Inactivation Date | 2020-01-31 |