NDC 69517-143 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69517-143 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-10-02 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-10-02 |
| Inactivation Date | 2020-01-31 |