NDC 49035-102 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49035-102 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part331 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-10-07 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part331 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-09-16 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-04-11 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | OTC monograph final |
| Application Number | part333E |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-04-07 |
| Marketing Category | OTC monograph final |
| Application Number | part331 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-09-22 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part331 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-09-22 |
| Inactivation Date | 2020-01-31 |