PROPOLIS50g (ATOMY CO., LTD.)
Welcome to the PulseAid listing for the PROPOLIS drug offered from ATOMY CO., LTD.. 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: | ATOMY CO., LTD. |
| NON-PROPRIETARY NAME: | SODIUM MONOFLUOROPHOSPHATE |
| SUBSTANCE NAME: | SODIUM MONOFLUOROPHOSPHATE; SODIUM FLUORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | DENTAL |
| DOSAGE FORM: | PASTE, DENTIFRICE |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2010-05-25 |
| END MARKETING DATE: | 0000-00-00 |
PROPOLIS 50g HUMAN OTC DRUG Details:
| Item Description | PROPOLIS 50g from ATOMY CO., LTD. |
| LABELER NAME: | ATOMY CO., LTD. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | .08; .05(g/50g; g/50g) |
| START MARKETING DATE: | 2010-05-25 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 52257-1208_a47b5a6d-b4fc-41b4-ba7a-df0b33cadc05 |
| PRODUCT NDC: | 52257-1208 |
| APPLICATION NUMBER: | part355 |
Other SODIUM MONOFLUOROPHOSPHATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers:
