ATOMY PROPOLIS50g (ATOMY CO., LTD.)
Welcome to the PulseAid listing for the ATOMY 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, Sodium Fluoride |
SUBSTANCE NAME: | SODIUM MONOFLUOROPHOSPHATE; SODIUM FLUORIDE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | PASTE, DENTIFRICE |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2015-02-01 |
END MARKETING DATE: | 0000-00-00 |
ATOMY PROPOLIS 50g HUMAN OTC DRUG Details:
Item Description | ATOMY PROPOLIS 50g from ATOMY CO., LTD. |
LABELER NAME: | ATOMY CO., LTD. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | .08; .05(g/41; g/41) |
START MARKETING DATE: | 2015-02-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52257-1310_c6b5bd0d-d969-40b0-a7ac-650593f1530c |
PRODUCT NDC: | 52257-1310 |
APPLICATION NUMBER: | part355 |
Other SODIUM MONOFLUOROPHOSPHATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers: