NDC 37000-831 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 37000-831 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-02-20 |
| Marketing End Date | 2015-03-22 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-02-20 |
| Marketing End Date | 2015-03-22 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-02-20 |
| Marketing End Date | 2015-03-22 |