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Colgate - 35000-067-60 - (Sodium Fluoride and Potassium Nitrate)
Drug Information of Colgate
| Product NDC: | 35000-067 |
| Proprietary Name: | Colgate |
| Non Proprietary Name: | Sodium Fluoride and Potassium Nitrate |
| Active Ingredient(s): | 50; 2.4 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
| Product NDC: | 35000-067 |
| Labeler Name: | Colgate-Palmolive |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121017 |
Package Information of Colgate
| Package NDC: | 35000-067-60 |
| Package Description: | 1 TUBE in 1 CARTON (35000-067-60) > 170 g in 1 TUBE |
NDC Information of Colgate
| NDC Code | 35000-067-60 |
| Proprietary Name | Colgate |
| Package Description | 1 TUBE in 1 CARTON (35000-067-60) > 170 g in 1 TUBE |
| Product NDC | 35000-067 |
| 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 | 20121017 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Colgate-Palmolive |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 50; 2.4 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
