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 DescriptionATOMY PROPOLIS 50g from ATOMY CO., LTD.
LABELER NAME: ATOMY CO., LTD.
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
ATOMY CO., LTD.PROPOLIS