NDC 54868-6233 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-6233 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-02-16 |
| Inactivation Date | 2019-09-24 |