NDC 75181-002 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 75181-002 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2020-05-13 |
| Marketing End Date | 2020-05-20 |