Product NDC: | 65954-553 |
Proprietary Name: | Colgate Sensitive Pro Relief Enamel Repair |
Non Proprietary Name: | SODIUM FLUORIDE and POTASSIUM NITRATE |
Active Ingredient(s): | 50; 1.5 mg/g; mg/g & nbsp; SODIUM FLUORIDE and POTASSIUM NITRATE |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65954-553 |
Labeler Name: | Mission Hills S.A de C.V |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110112 |
Package NDC: | 65954-553-01 |
Package Description: | 1 TUBE in 1 CARTON (65954-553-01) > 28.3 g in 1 TUBE |
NDC Code | 65954-553-01 |
Proprietary Name | Colgate Sensitive Pro Relief Enamel Repair |
Package Description | 1 TUBE in 1 CARTON (65954-553-01) > 28.3 g in 1 TUBE |
Product NDC | 65954-553 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM FLUORIDE and POTASSIUM NITRATE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20110112 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Mission Hills S.A de C.V |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | 50; 1.5 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |