Fluor-a-day (Arbor Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the Fluor-a-day drug offered from Arbor Pharmaceuticals, Inc.. This pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Arbor Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: Sodium fluoride and Xylitol
SUBSTANCE NAME: SODIUM FLUORIDE; XYLITOL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, CHEWABLE
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2010-08-15
END MARKETING DATE: 0000-00-00


Fluor-a-day HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFluor-a-day from Arbor Pharmaceuticals, Inc.
LABELER NAME: Arbor Pharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: .25; 236.79(mg/1; mg/1)
START MARKETING DATE: 2010-08-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24338-602_935d5be5-4713-4114-8c99-a50c953b1fee
PRODUCT NDC: 24338-602
APPLICATION NUMBER:

Other SODIUM FLUORIDE; XYLITOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Arbor Pharmaceuticals, Inc.Fluor-a-day