ATOMY PROPOLIS TOOTHPAS TE 50g (ATOMY CO., LTD.)


Welcome to the PulseAid listing for the ATOMY PROPOLIS TOOTHPAS TE 50g 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: 2016-08-01
END MARKETING DATE: 0000-00-00


ATOMY PROPOLIS TOOTHPAS TE 50g HUMAN OTC DRUG Details:

Item DescriptionATOMY PROPOLIS TOOTHPAS TE 50g from ATOMY CO., LTD.
LABELER NAME: ATOMY CO., LTD.
DEA SCHEDULE:
ACTIVE STRENGTH: .08; .05(g/50g; g/50g)
START MARKETING DATE: 2016-08-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 52257-1350_0863b8d7-55a2-4cc4-aa40-596625ca2124
PRODUCT NDC: 52257-1350
APPLICATION NUMBER: part355

Other SODIUM MONOFLUOROPHOSPHATE; SODIUM FLUORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
ATOMY CO., LTD.PROPOLIS