SensodyneFresh Mint (GlaxoSmithKline Consumer Healthcare Holdings (US) LLC)
Welcome to the PulseAid listing for the Sensodyne drug offered from GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. 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: | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| NON-PROPRIETARY NAME: | potassium nitrate and sodium fluoride |
| 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: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
Sensodyne Fresh Mint HUMAN OTC DRUG Details:
| Item Description | Sensodyne Fresh Mint from GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| LABELER NAME: | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50; 1.5(mg/g; mg/g) |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0135-0529_e1205168-1a5c-4e3e-b7a9-6b7c3d683de6 |
| PRODUCT NDC: | 0135-0529 |
| APPLICATION NUMBER: | part356 |
Other POTASSIUM NITRATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers:
