Product NDC: | 51442-536 |
Proprietary Name: | Colgate Triple Action Original Mint Fluoride |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | 2.4 mg/g & nbsp; Sodium Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51442-536 |
Labeler Name: | Colgate-Palmolive Canada |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100407 |
Package NDC: | 51442-536-64 |
Package Description: | 1 TUBE in 1 CARTON (51442-536-64) > 181 g in 1 TUBE |
NDC Code | 51442-536-64 |
Proprietary Name | Colgate Triple Action Original Mint Fluoride |
Package Description | 1 TUBE in 1 CARTON (51442-536-64) > 181 g in 1 TUBE |
Product NDC | 51442-536 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20100407 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Colgate-Palmolive Canada |
Substance Name | SODIUM FLUORIDE |
Strength Number | 2.4 |
Strength Unit | mg/g |
Pharmaceutical Classes |