Hello (Hello Products LLC)
Welcome to the PulseAid listing for the Hello drug offered from Hello Products LLC. 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: | Hello Products LLC |
NON-PROPRIETARY NAME: | Potassium nitrate and Sodium fluoride |
SUBSTANCE NAME: | POTASSIUM NITRATE; SODIUM FLUORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | PASTE, DENTIFRICE |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2017-02-15 |
END MARKETING DATE: | 0000-00-00 |
Hello HUMAN OTC DRUG Details:
Item Description | Hello from Hello Products LLC |
LABELER NAME: | Hello Products LLC |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 50; 1.5(mg/g; mg/g) |
START MARKETING DATE: | 2017-02-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 55882-6097_95456c75-458d-46b5-920f-05230dd46eed |
PRODUCT NDC: | 55882-6097 |
APPLICATION NUMBER: | part356 |
Other POTASSIUM NITRATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers: