PreviDent 5000 Enamel Protect (Colgate Oral Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the PreviDent 5000 Enamel Protect drug offered from Colgate Oral Pharmaceuticals, Inc.. This 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 Oral Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | SODIUM FLUORIDE and POTASSIUM NITRATE |
SUBSTANCE NAME: | SODIUM FLUORIDE; POTASSIUM NITRATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | GEL, DENTIFRICE |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2011-03-30 |
END MARKETING DATE: | 0000-00-00 |
PreviDent 5000 Enamel Protect HUMAN PRESCRIPTION DRUG Details:
Item Description | PreviDent 5000 Enamel Protect from Colgate Oral Pharmaceuticals, Inc. |
LABELER NAME: | Colgate Oral Pharmaceuticals, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 12.7; 57.5(mg/mL; mg/mL) |
START MARKETING DATE: | 2011-03-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0126-0022_430a6a1e-1089-4626-8965-c0875303b4f2 |
PRODUCT NDC: | 0126-0022 |
APPLICATION NUMBER: | |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers: