PROTOXIN (PROTOX Inc.)
Welcome to the PulseAid listing for the PROTOXIN drug offered from PROTOX 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: | PROTOX Inc. |
| NON-PROPRIETARY NAME: | Clostridium botulinum Toxin Type A |
| SUBSTANCE NAME: | CLOSTRIDIUM BOTULINUM |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | GEL |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2016-11-10 |
| END MARKETING DATE: | 0000-00-00 |
PROTOXIN HUMAN OTC DRUG Details:
| Item Description | PROTOXIN from PROTOX Inc. |
| LABELER NAME: | PROTOX Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(g/10mL) |
| START MARKETING DATE: | 2016-11-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 71066-0001_41280d2a-9232-5800-e054-00144ff88e88 |
| PRODUCT NDC: | 71066-0001 |
| APPLICATION NUMBER: | |
Other CLOSTRIDIUM BOTULINUM Pharmaceutical Manufacturers / Labelers:
