Colgate Total Whitening (Colgate-Palmolive)


Welcome to the PulseAid listing for the Colgate Total Whitening drug offered from Colgate-Palmolive. 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: Colgate-Palmolive
NON-PROPRIETARY NAME: Sodium Fluoride and Triclosan
SUBSTANCE NAME: SODIUM FLUORIDE; TRICLOSAN
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: DENTAL
DOSAGE FORM: PASTE, DENTIFRICE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2010-09-20
END MARKETING DATE: 0000-00-00


Colgate Total Whitening HUMAN OTC DRUG Details:

Item DescriptionColgate Total Whitening from Colgate-Palmolive
LABELER NAME: Colgate-Palmolive
DEA SCHEDULE:
ACTIVE STRENGTH: 1.4; 3(mg/g; mg/g)
START MARKETING DATE: 2010-09-20
END MARKETING DATE: 0000-00-00
PRODUCT ID: 35000-002_1305038a-e3a5-4358-84f9-49a4bb286804
PRODUCT NDC: 35000-002
APPLICATION NUMBER: NDA020231

Other SODIUM FLUORIDE; TRICLOSAN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Colgate-PalmoliveColgate
Colgate-Palmolive CompanyColgate
Mission Hills, S.A. de C.V.Colgate
Navajo Manufacturing Company IncColgate Total Clean Mint ANTIGINGIVITIS
Team Technologies, IncTotal Whitening