ColgateTotal Gum Defense (Colgate-Palmolive)


Welcome to the PulseAid listing for the Colgate 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: Silicon Dioxide, Sodium Fluoride, and Triclosan
SUBSTANCE NAME: SILICON DIOXIDE; SODIUM FLUORIDE; TRICLOSAN
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: DENTAL
DOSAGE FORM: PASTE, DENTIFRICE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2011-06-25
END MARKETING DATE: 0000-00-00


Colgate Total Gum Defense HUMAN OTC DRUG Details:

Item DescriptionColgate Total Gum Defense from Colgate-Palmolive
LABELER NAME: Colgate-Palmolive
DEA SCHEDULE:
ACTIVE STRENGTH: 50; 2.4; 3(mg/g; mg/g; mg/g)
START MARKETING DATE: 2011-06-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 35000-048_0e814ed4-428b-4f06-a27a-3d0196cb0eb6
PRODUCT NDC: 35000-048
APPLICATION NUMBER: NDA020231

Other SILICON DIOXIDE; SODIUM FLUORIDE; TRICLOSAN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Colgate-PalmoliveColgate
Colgate-Palmolive CompanyColgate