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

Manufacturer / LabelerProprietary Name
ATOMY CO., LTD.PROPOLIS