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Colgate - 51442-552-20 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of Colgate
| Product NDC: | 51442-552 |
| Proprietary Name: | Colgate |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | 7.6 mg/g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Colgate
| Product NDC: | 51442-552 |
| Labeler Name: | Colgate-Palmolive Canada |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110606 |
Package Information of Colgate
| Package NDC: | 51442-552-20 |
| Package Description: | 24 g in 1 TUBE (51442-552-20) |
NDC Information of Colgate
| NDC Code | 51442-552-20 |
| Proprietary Name | Colgate |
| Package Description | 24 g in 1 TUBE (51442-552-20) |
| Product NDC | 51442-552 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20110606 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Colgate-Palmolive Canada |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 7.6 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
