PreviDent5000 Sensitive (Colgate-Palmolive Company)
Welcome to the PulseAid listing for the PreviDent drug offered from Colgate-Palmolive Company. This Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Colgate-Palmolive Company |
| NON-PROPRIETARY NAME: | Sodium fluoride |
| SUBSTANCE NAME: | SODIUM FLUORIDE; POTASSIUM NITRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
| ROUTE: | DENTAL |
| DOSAGE FORM: | GEL, DENTIFRICE |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2009-07-06 |
| END MARKETING DATE: | 0000-00-00 |
PreviDent 5000 Sensitive HUMAN PRESCRIPTION DRUG Details:
| Item Description | PreviDent 5000 Sensitive from Colgate-Palmolive Company |
| LABELER NAME: | Colgate-Palmolive Company |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 12.7; 57.5(mg/mL; mg/mL) |
| START MARKETING DATE: | 2009-07-06 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0126-0070_e4aefcbf-56d5-457e-8dbc-7704f5b3ed36 |
| PRODUCT NDC: | 0126-0070 |
| APPLICATION NUMBER: | |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers:
