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Colgate Sensitive Pro Relief
Colgate Sensitive Pro Relief - 65954-549-69 - (SODIUM FLUORIDE and POTASSIUM NITRATE)
Drug Information of Colgate Sensitive Pro Relief
| Product NDC: | 65954-549 |
| Proprietary Name: | Colgate Sensitive Pro Relief |
| Non Proprietary Name: | SODIUM FLUORIDE and POTASSIUM NITRATE |
| Active Ingredient(s): | 50; 1.1 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) |
Labeler Information of Colgate Sensitive Pro Relief
| Product NDC: | 65954-549 |
| Labeler Name: | Mission Hills S.A de C.V |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100906 |
Package Information of Colgate Sensitive Pro Relief
| Package NDC: | 65954-549-69 |
| Package Description: | 1 TUBE in 1 CARTON (65954-549-69) > 113 g in 1 TUBE |
NDC Information of Colgate Sensitive Pro Relief
| NDC Code | 65954-549-69 |
| Proprietary Name | Colgate Sensitive Pro Relief |
| Package Description | 1 TUBE in 1 CARTON (65954-549-69) > 113 g in 1 TUBE |
| Product NDC | 65954-549 |
| 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 | 20100906 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Mission Hills S.A de C.V |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 50; 1.1 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
