NDC 41163-020 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 41163-020 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2009-11-18 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-05-08 |