SENSITIVE ANTI-CAVITY (Universal Distribution Center LLC)
Welcome to the PulseAid listing for the SENSITIVE ANTI-CAVITY drug offered from Universal Distribution Center 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: | Universal Distribution Center LLC |
| NON-PROPRIETARY NAME: | potassium nitrate and sodium fluoride |
| SUBSTANCE NAME: | POTASSIUM NITRATE; SODIUM FLUORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | PASTE |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2017-06-21 |
| END MARKETING DATE: | 0000-00-00 |
SENSITIVE ANTI-CAVITY HUMAN OTC DRUG Details:
| Item Description | SENSITIVE ANTI-CAVITY from Universal Distribution Center LLC |
| LABELER NAME: | Universal Distribution Center LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50; 1.5(mg/g; mg/g) |
| START MARKETING DATE: | 2017-06-21 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 52000-037_527d601e-591a-38fb-e054-00144ff8d46c |
| PRODUCT NDC: | 52000-037 |
| APPLICATION NUMBER: | part356 |
Other POTASSIUM NITRATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers:
