Iodent Sensitive Extra Whitening (United Exchange Corp.)
Welcome to the PulseAid listing for the Iodent Sensitive Extra Whitening 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: | Sodium Fluoride Potassium Nitrate |
SUBSTANCE NAME: | SODIUM FLUORIDE; POTASSIUM NITRATE |
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 Extra Whitening HUMAN OTC DRUG Details:
Item Description | Iodent Sensitive Extra Whitening from United Exchange Corp. |
LABELER NAME: | United Exchange Corp. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5; 2.43(mg/g; mg/g) |
START MARKETING DATE: | 2014-10-23 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 65923-105_d5a39bc5-33ee-4851-a33b-5ddcb523b129 |
PRODUCT NDC: | 65923-105 |
APPLICATION NUMBER: | part356 |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers: