Opalescence Sensitivity Relief Whitening (Ultradent Products, Inc.)
Welcome to the PulseAid listing for the Opalescence Sensitivity Relief Whitening 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: | Potassium Nitrate and Sodium Fluoride |
SUBSTANCE NAME: | POTASSIUM NITRATE; SODIUM FLUORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | GEL, DENTIFRICE |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2015-11-30 |
END MARKETING DATE: | 0000-00-00 |
Opalescence Sensitivity Relief Whitening HUMAN OTC DRUG Details:
Item Description | Opalescence Sensitivity Relief Whitening from Ultradent Products, Inc. |
LABELER NAME: | Ultradent Products, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 50; 2.5(mg/g; mg/g) |
START MARKETING DATE: | 2015-11-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51206-308_45c1c632-30ea-4797-ae47-9e987250543e |
PRODUCT NDC: | 51206-308 |
APPLICATION NUMBER: | part356 |
Other POTASSIUM NITRATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers: