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Vortex
Vortex - 52316-028-42 - (Toothpaste)
Drug Information of Vortex
| Product NDC: | 52316-028 |
| Proprietary Name: | Vortex |
| Non Proprietary Name: | Toothpaste |
| Active Ingredient(s): | 2 mg/g & nbsp; Toothpaste |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vortex
| Product NDC: | 52316-028 |
| Labeler Name: | DSC Laboratories, Div. of DSC Products Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111230 |
Package Information of Vortex
| Package NDC: | 52316-028-42 |
| Package Description: | 120 g in 1 TUBE (52316-028-42) |
NDC Information of Vortex
| NDC Code | 52316-028-42 |
| Proprietary Name | Vortex |
| Package Description | 120 g in 1 TUBE (52316-028-42) |
| Product NDC | 52316-028 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Toothpaste |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20111230 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DSC Laboratories, Div. of DSC Products Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
