NDC 0182-1061 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0182-1061 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1994-02-05 |
| Marketing End Date | 2013-05-30 |