Colgate Enamel Health Sensitivity Relief (Colgate-Palmolive)
Welcome to the PulseAid listing for the Colgate Enamel Health Sensitivity Relief drug offered from Colgate-Palmolive. 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: | Colgate-Palmolive |
NON-PROPRIETARY NAME: | POTASSIUM NITRATE and SODIUM FLUORIDE |
SUBSTANCE NAME: | POTASSIUM NITRATE; SODIUM FLUORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | GEL, DENTIFRICE |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2014-06-30 |
END MARKETING DATE: | 0000-00-00 |
Colgate Enamel Health Sensitivity Relief HUMAN OTC DRUG Details:
Item Description | Colgate Enamel Health Sensitivity Relief from Colgate-Palmolive |
LABELER NAME: | Colgate-Palmolive |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 50; 2.4(mg/g; mg/g) |
START MARKETING DATE: | 2014-06-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 35000-206_8536b89f-efcc-479b-af89-8b7c683fb400 |
PRODUCT NDC: | 35000-206 |
APPLICATION NUMBER: | part356 |
Other POTASSIUM NITRATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers: