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 |