| 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: | 65954-536-79 | 
| Package Description: | 1 TUBE in 1 CARTON (65954-536-79) > 79 g in 1 TUBE | 
| NDC Code | 65954-536-79 | 
| Proprietary Name | Colgate Triple Action | 
| Package Description | 1 TUBE in 1 CARTON (65954-536-79) > 79 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 |