WakefernMaximum Strength (Wakefern)
Welcome to the PulseAid listing for the Wakefern drug offered from Wakefern. 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: | Wakefern |
| NON-PROPRIETARY NAME: | 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: | 2013-06-03 |
| END MARKETING DATE: | 0000-00-00 |
Wakefern Maximum Strength HUMAN OTC DRUG Details:
| Item Description | Wakefern Maximum Strength from Wakefern |
| LABELER NAME: | Wakefern |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | .24; 5(g/100g; g/100g) |
| START MARKETING DATE: | 2013-06-03 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 41190-207_ba1b54b8-f747-46dd-95cd-435450d7b43f |
| PRODUCT NDC: | 41190-207 |
| APPLICATION NUMBER: | part356 |
Other SODIUM FLUORIDE; POTASSIUM NITRATE Pharmaceutical Manufacturers / Labelers:
