OMNI (3M ESPE Dental Products)
Welcome to the PulseAid listing for the OMNI drug offered from 3M ESPE Dental Products. 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: | 3M ESPE Dental Products |
NON-PROPRIETARY NAME: | stannous fluoride |
SUBSTANCE NAME: | STANNOUS FLUORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | GEL |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 1998-02-01 |
END MARKETING DATE: | 0000-00-00 |
OMNI HUMAN OTC DRUG Details:
Item Description | OMNI from 3M ESPE Dental Products |
LABELER NAME: | 3M ESPE Dental Products |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 0.969(mg/g) |
START MARKETING DATE: | 1998-02-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 48878-4061_2b66401d-24b1-4074-9255-64da3b8cb506 |
PRODUCT NDC: | 48878-4061 |
APPLICATION NUMBER: | part355 |
Other STANNOUS FLUORIDE Pharmaceutical Manufacturers / Labelers: