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: