SprinJene NaturalSensitivity Relief (Health and Natural Beauty USA Corp)
Welcome to the PulseAid listing for the SprinJene Natural drug offered from Health and Natural Beauty USA Corp. 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: | Health and Natural Beauty USA Corp |
| NON-PROPRIETARY NAME: | Sodium Monofluorophosphate and Potassium Nitrate |
| SUBSTANCE NAME: | SODIUM MONOFLUOROPHOSPHATE; POTASSIUM NITRATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | DENTAL |
| DOSAGE FORM: | PASTE, DENTIFRICE |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2017-07-01 |
| END MARKETING DATE: | 0000-00-00 |
SprinJene Natural Sensitivity Relief HUMAN OTC DRUG Details:
| Item Description | SprinJene Natural Sensitivity Relief from Health and Natural Beauty USA Corp |
| LABELER NAME: | Health and Natural Beauty USA Corp |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1.5; 50(mg/g; mg/g) |
| START MARKETING DATE: | 2017-07-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63404-1942_c00995ff-76f6-4ec9-ad97-a9c4e911e284 |
| PRODUCT NDC: | 63404-1942 |
| APPLICATION NUMBER: | part356 |
Other SODIUM MONOFLUOROPHOSPHATE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers:
