Pro-Den Rx (Den-mat Holdings, Llc)
Welcome to the PulseAid listing for the Pro-Den Rx drug offered from Den-mat Holdings, Llc. 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: | Den-mat Holdings, Llc |
| NON-PROPRIETARY NAME: | Stannous Fluoride |
| SUBSTANCE NAME: | STANNOUS FLUORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | GEL |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2008-10-31 |
| END MARKETING DATE: | 0000-00-00 |
Pro-Den Rx HUMAN OTC DRUG Details:
| Item Description | Pro-Den Rx from Den-mat Holdings, Llc |
| LABELER NAME: | Den-mat Holdings, Llc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1.8(g/g) |
| START MARKETING DATE: | 2008-10-31 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 59883-720_7191e845-ca7b-451e-b43e-dba3ca59f6b5 |
| PRODUCT NDC: | 59883-720 |
| APPLICATION NUMBER: | |
Other STANNOUS FLUORIDE Pharmaceutical Manufacturers / Labelers:
