Product NDC: | 67751-131 |
Proprietary Name: | Colgate Total Clean Mint ANTIGINGIVITIS |
Non Proprietary Name: | SODIUM FLUORIDE |
Active Ingredient(s): | .14; .3 g/100g; g/100g & nbsp; SODIUM FLUORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67751-131 |
Labeler Name: | Navajo Manufacturing Company Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA020231 |
Marketing Category: | NDA |
Start Marketing Date: | 20130624 |
Package NDC: | 67751-131-01 |
Package Description: | 1 TUBE in 1 PACKAGE (67751-131-01) > 21.2 g in 1 TUBE |
NDC Code | 67751-131-01 |
Proprietary Name | Colgate Total Clean Mint ANTIGINGIVITIS |
Package Description | 1 TUBE in 1 PACKAGE (67751-131-01) > 21.2 g in 1 TUBE |
Product NDC | 67751-131 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM FLUORIDE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | ORAL |
Start Marketing Date | 20130624 |
Marketing Category Name | NDA |
Labeler Name | Navajo Manufacturing Company Inc |
Substance Name | SODIUM FLUORIDE; TRICLOSAN |
Strength Number | .14; .3 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |