NDC 67618-100 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67618-100 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1997-01-30 |
| Marketing End Date | 2012-12-05 |
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-30 |
| Marketing End Date | 2016-08-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-01-30 |
| Marketing End Date | 2016-08-31 |