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: