iBrite (Pac-Dent International Inc.)
Welcome to the PulseAid listing for the iBrite drug offered from Pac-Dent International 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: | Pac-Dent International Inc. |
| NON-PROPRIETARY NAME: | Sodium Fluoride, Potassium Nitrate |
| SUBSTANCE NAME: | SODIUM FLUORIDE; POTASSIUM NITRATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | PASTE, DENTIFRICE |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2016-02-01 |
| END MARKETING DATE: | 0000-00-00 |
iBrite HUMAN OTC DRUG Details:
| Item Description | iBrite from Pac-Dent International Inc. |
| LABELER NAME: | Pac-Dent International Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2.54; 30(mg/g; mg/g) |
| START MARKETING DATE: | 2016-02-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68983-006_25f0e453-ed77-141b-e054-00144ff8d46c |
| PRODUCT NDC: | 68983-006 |
| APPLICATION NUMBER: | part356 |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers:
