| 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 |