Product NDC: | 67751-132 |
Proprietary Name: | Colgate Cavity Protection Tooth |
Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
Active Ingredient(s): | .76 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67751-132 |
Labeler Name: | Navajo Manufacturing Company Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130531 |
Package NDC: | 67751-132-01 |
Package Description: | 1 TUBE in 1 CARTON (67751-132-01) > 24 g in 1 TUBE |
NDC Code | 67751-132-01 |
Proprietary Name | Colgate Cavity Protection Tooth |
Package Description | 1 TUBE in 1 CARTON (67751-132-01) > 24 g in 1 TUBE |
Product NDC | 67751-132 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20130531 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Navajo Manufacturing Company Inc |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | .76 |
Strength Unit | g/100g |
Pharmaceutical Classes |