HEBExtra Whitening (HEB)
Welcome to the PulseAid listing for the HEB drug offered from HEB. 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: | HEB |
| NON-PROPRIETARY NAME: | Fluoride |
| SUBSTANCE NAME: | SODIUM FLUORIDE; POTASSIUM NITRATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | DENTAL |
| DOSAGE FORM: | PASTE, DENTIFRICE |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2011-01-20 |
| END MARKETING DATE: | 0000-00-00 |
HEB Extra Whitening HUMAN OTC DRUG Details:
| Item Description | HEB Extra Whitening from HEB |
| LABELER NAME: | HEB |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 1.5; 5(g/g; g/g) |
| START MARKETING DATE: | 2011-01-20 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 37808-861_64accd4a-9481-4cc8-902a-5497c01fb37a |
| PRODUCT NDC: | 37808-861 |
| APPLICATION NUMBER: | part356 |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers:
