Crest 3DWhite Whitening TherapySensitivity Care (The Procter & Gamble Manufacturing Company)
Welcome to the PulseAid listing for the Crest 3DWhite Whitening Therapy 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: | Potassium Nitrate, Sodium Fluoride |
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: | 2017-07-12 |
END MARKETING DATE: | 0000-00-00 |
Crest 3DWhite Whitening Therapy Sensitivity Care HUMAN OTC DRUG Details:
Item Description | Crest 3DWhite Whitening Therapy Sensitivity Care 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: | 2017-07-12 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 37000-456_5422c453-58e5-687c-e054-00144ff88e88 |
PRODUCT NDC: | 37000-456 |
APPLICATION NUMBER: | part356 |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers: