Iodent Sensitive Fresh Mint (United Exchange Corp.)
Welcome to the PulseAid listing for the Iodent Sensitive Fresh Mint drug offered from United Exchange 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: | United Exchange Corp. |
NON-PROPRIETARY NAME: | Potassium nitrate and sodium floride |
SUBSTANCE NAME: | POTASSIUM NITRATE; SODIUM FLUORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | PASTE |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2014-10-23 |
END MARKETING DATE: | 0000-00-00 |
Iodent Sensitive Fresh Mint HUMAN OTC DRUG Details:
Item Description | Iodent Sensitive Fresh Mint from United Exchange Corp. |
LABELER NAME: | United Exchange Corp. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 5; .15(mg/100g; mg/100g) |
START MARKETING DATE: | 2014-10-23 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 65923-101_9fb471d5-d147-4a7a-8f57-0690e8249f36 |
PRODUCT NDC: | 65923-101 |
APPLICATION NUMBER: | part356 |
Other POTASSIUM NITRATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers: