NDC 35658-000 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 35658-000 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part333D |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-07-01 |
| Inactivation Date | 2019-10-21 |