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PreviDent
PreviDent - 0126-0179-16 - (Sodium Fluoride)
Drug Information of PreviDent
| Product NDC: | 0126-0179 |
| Proprietary Name: | PreviDent |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 2 mg/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PreviDent
| Product NDC: | 0126-0179 |
| Labeler Name: | Colgate Oral Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120829 |
Package Information of PreviDent
| Package NDC: | 0126-0179-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0126-0179-16) |
NDC Information of PreviDent
| NDC Code | 0126-0179-16 |
| Proprietary Name | PreviDent |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (0126-0179-16) |
| Product NDC | 0126-0179 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | MOUTHWASH |
| Route Name | DENTAL |
| Start Marketing Date | 20120829 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Colgate Oral Pharmaceuticals, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
