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PreviDent 5000 Enamel Protect
PreviDent 5000 Enamel Protect - 0126-0022-92 - (SODIUM FLUORIDE and POTASSIUM NITRATE)
Drug Information of PreviDent 5000 Enamel Protect
| Product NDC: | 0126-0022 |
| Proprietary Name: | PreviDent 5000 Enamel Protect |
| Non Proprietary Name: | SODIUM FLUORIDE and POTASSIUM NITRATE |
| Active Ingredient(s): | 57.5; 12.7 mg/mL; mg/mL & nbsp; SODIUM FLUORIDE and POTASSIUM NITRATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PreviDent 5000 Enamel Protect
| Product NDC: | 0126-0022 |
| Labeler Name: | Colgate Oral Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110330 |
Package Information of PreviDent 5000 Enamel Protect
| Package NDC: | 0126-0022-92 |
| Package Description: | 100 mL in 1 BOTTLE (0126-0022-92) |
NDC Information of PreviDent 5000 Enamel Protect
| NDC Code | 0126-0022-92 |
| Proprietary Name | PreviDent 5000 Enamel Protect |
| Package Description | 100 mL in 1 BOTTLE (0126-0022-92) |
| Product NDC | 0126-0022 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM FLUORIDE and POTASSIUM NITRATE |
| Dosage Form Name | GEL, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20110330 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Colgate Oral Pharmaceuticals, Inc. |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 57.5; 12.7 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
