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: | STANNOUS FLUORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | PASTE, DENTIFRICE |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-12-01 |
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: | 0.454(g/100g) |
START MARKETING DATE: | 2012-12-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 37808-171_7f40fc97-a527-448b-858f-d5052a48160b |
PRODUCT NDC: | 37808-171 |
APPLICATION NUMBER: | part355 |
Other STANNOUS FLUORIDE Pharmaceutical Manufacturers / Labelers: