| Product NDC: | 0126-0027 |
| Proprietary Name: | Colgate Cavity Protection |
| Non Proprietary Name: | Sodium Monofluorophosphate |
| Active Ingredient(s): | 11.4 mg/g & nbsp; Sodium Monofluorophosphate |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0126-0027 |
| Labeler Name: | Colgate Oral Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120203 |
| Package NDC: | 0126-0027-44 |
| Package Description: | 4.25 g in 1 POUCH (0126-0027-44) |
| NDC Code | 0126-0027-44 |
| Proprietary Name | Colgate Cavity Protection |
| Package Description | 4.25 g in 1 POUCH (0126-0027-44) |
| Product NDC | 0126-0027 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Monofluorophosphate |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20120203 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Colgate Oral Pharmaceuticals, Inc. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 11.4 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |