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: