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: |
|
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: