NUMOTIZINE (Hobart Laboratories, Inc.)
Welcome to the PulseAid listing for the NUMOTIZINE drug offered from Hobart Laboratories, Inc.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Hobart Laboratories, Inc. |
| NON-PROPRIETARY NAME: | MENTHOL |
| SUBSTANCE NAME: | MENTHOL |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | OINTMENT |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2011-11-30 |
| END MARKETING DATE: | 0000-00-00 |
NUMOTIZINE HUMAN OTC DRUG Details:
| Item Description | NUMOTIZINE from Hobart Laboratories, Inc. |
| LABELER NAME: | Hobart Laboratories, Inc. |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | 1.25(g/100g) |
| START MARKETING DATE: | 2011-11-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 10546-100_d4255df9-25b6-4373-9b04-827605029434 |
| PRODUCT NDC: | 10546-100 |
| APPLICATION NUMBER: | part348 |