Goodsense Sensitive Extra Whitening (Geiss, Destin & Dunn, Inc.)
Welcome to the PulseAid listing for the Goodsense Sensitive Extra Whitening drug offered from Geiss, Destin & Dunn, Inc.. 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: | Geiss, Destin & Dunn, Inc. |
| NON-PROPRIETARY NAME: | Potassium Nitrate, and Sodium Fluroide |
| SUBSTANCE NAME: | POTASSIUM NITRATE; SODIUM FLUORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | PASTE |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2015-12-29 |
| END MARKETING DATE: | 0000-00-00 |
Goodsense Sensitive Extra Whitening HUMAN OTC DRUG Details:
| Item Description | Goodsense Sensitive Extra Whitening from Geiss, Destin & Dunn, Inc. |
| LABELER NAME: | Geiss, Destin & Dunn, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50; 1.5(mg/g; mg/g) |
| START MARKETING DATE: | 2015-12-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50804-780_4c20b60b-4a1e-4033-9a71-f1cd226cb8cf |
| PRODUCT NDC: | 50804-780 |
| APPLICATION NUMBER: | part356 |
Other POTASSIUM NITRATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers:
