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Pro-Den Rx
Pro-Den Rx - 59883-821-02 - (Sodium Fluoride)
Drug Information of Pro-Den Rx
| Product NDC: | 59883-821 |
| Proprietary Name: | Pro-Den Rx |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 4.3 g/g & nbsp; Sodium Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pro-Den Rx
| Product NDC: | 59883-821 |
| Labeler Name: | Zila Therapeutics, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20081121 |
Package Information of Pro-Den Rx
| Package NDC: | 59883-821-02 |
| Package Description: | 1 TUBE in 1 CARTON (59883-821-02) > 56 g in 1 TUBE |
NDC Information of Pro-Den Rx
| NDC Code | 59883-821-02 |
| Proprietary Name | Pro-Den Rx |
| Package Description | 1 TUBE in 1 CARTON (59883-821-02) > 56 g in 1 TUBE |
| Product NDC | 59883-821 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | GEL |
| Route Name | ORAL |
| Start Marketing Date | 20081121 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Zila Therapeutics, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 4.3 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
