NDC 47682-116 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 47682-116 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-12-30 |
| Marketing End Date | 2013-08-30 |
| Marketing Category | OTC monograph final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-12-30 |
| Marketing End Date | 2013-08-30 |
| Marketing Category | OTC monograph final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-12-30 |
| Marketing End Date | 2013-08-30 |
| Marketing Category | OTC monograph final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-12-30 |
| Marketing End Date | 2013-08-30 |