Opalescence PF (Ultradent Products, Inc.)
Welcome to the PulseAid listing for the Opalescence PF drug offered from Ultradent Products, 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: | Ultradent Products, Inc. |
| NON-PROPRIETARY NAME: | Sodium Fluoride and Potassium Nitrate |
| SUBSTANCE NAME: | SODIUM FLUORIDE; POTASSIUM NITRATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | DENTAL |
| DOSAGE FORM: | PASTE, DENTIFRICE |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2010-11-15 |
| END MARKETING DATE: | 0000-00-00 |
Opalescence PF HUMAN OTC DRUG Details:
| Item Description | Opalescence PF from Ultradent Products, Inc. |
| LABELER NAME: | Ultradent Products, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | .070875; 1.4175(g/28.35g; g/28.35g) |
| START MARKETING DATE: | 2010-11-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51206-303_cf9374d9-3fe6-456f-b447-b66386decefb |
| PRODUCT NDC: | 51206-303 |
| APPLICATION NUMBER: | part355 |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers:
