Crest Sensi-Namel (The Procter & Gamble Manufacturing Company)
Welcome to the PulseAid listing for the Crest Sensi-Namel drug offered from The Procter & Gamble Manufacturing Company. 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: | The Procter & Gamble Manufacturing Company |
NON-PROPRIETARY NAME: | Sodium Fluoride and Potassium Nitrate |
SUBSTANCE NAME: | SODIUM FLUORIDE; POTASSIUM NITRATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | PASTE, DENTIFRICE |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2014-07-01 |
END MARKETING DATE: | 2017-11-11 |
Crest Sensi-Namel HUMAN OTC DRUG Details:
Item Description | Crest Sensi-Namel from The Procter & Gamble Manufacturing Company |
LABELER NAME: | The Procter & Gamble Manufacturing Company |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1.4; 50(mg/g; mg/g) |
START MARKETING DATE: | 2014-07-01 |
END MARKETING DATE: | 2017-11-11 |
PRODUCT ID: | 37000-857_3eaf2fc1-1645-3546-e054-00144ff8d46c |
PRODUCT NDC: | 37000-857 |
APPLICATION NUMBER: | part356 |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers: