NDC 36800-829 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 36800-829 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-09 |
| Marketing End Date | 2015-10-21 |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-23 |
| Marketing End Date | 2015-10-21 |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-08 |
| Marketing End Date | 2015-09-16 |