| Product NDC: | 65954-536 |
| Proprietary Name: | Colgate Triple Action |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | 1.1 mg/g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65954-536 |
| 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: | 20101201 |
| Package NDC: | 65954-536-64 |
| Package Description: | 1 TUBE in 1 CARTON (65954-536-64) > 181 g in 1 TUBE |
| NDC Code | 65954-536-64 |
| Proprietary Name | Colgate Triple Action |
| Package Description | 1 TUBE in 1 CARTON (65954-536-64) > 181 g in 1 TUBE |
| Product NDC | 65954-536 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20101201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mission Hills S.A de C.V |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1.1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |