Alpha-Pro (Dental Technologies, Inc.)


Welcome to the PulseAid listing for the Alpha-Pro drug offered from Dental Technologies, 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: Dental Technologies, Inc.
NON-PROPRIETARY NAME: Sodium Fluoride and Hydrofluoric Acid
SUBSTANCE NAME: SODIUM FLUORIDE; HYDROFLUORIC ACID
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: DENTAL
DOSAGE FORM: GEL
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2013-04-01
END MARKETING DATE: 0000-00-00


Alpha-Pro HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAlpha-Pro from Dental Technologies, Inc.
LABELER NAME: Dental Technologies, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 7.9; 4.4(mg/g; mg/g)
START MARKETING DATE: 2013-04-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 55346-0942_5b7fbec6-ecf3-49e1-97b1-0c2c71488fcf
PRODUCT NDC: 55346-0942
APPLICATION NUMBER:

Other SODIUM FLUORIDE; HYDROFLUORIC ACID Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
AR Medicom IncDenti-Care
Dental Technologies, Inc.Alpha-Pro
Laclede, Inc.Topical Fluoride Foam Bumble Bee Bubble Gum
Oral-B LaboratoriesOral-B Minute-Foam Orang-A-Tangy
U.S.I.A. IncPhocal Apf
Young Dental Manufacturing Co 1, LLC.Perfect Choice