Pro-Den Rx - Sodium Fluoride
Navigation: NDC > Supplier starting with: Z > ZILA THERAPEUTICS, INC.| Field | Value |
|---|---|
| NDC Code: | 59883-721 |
| Proprietary Name: | Pro-Den Rx |
| Suffix: | |
| Non-Proprietary Name: | Sodium Fluoride |
| Dosage Form: | GEL |
| Method: | ORAL |
| Original Marketing Date: | 31-10-2008 |
| Category Name: | OTC MONOGRAPH FINAL |
| Application Number: | part355 |
| Labeler: | ZILA THERAPEUTICS, INC. |
| Substance Name: | STANNOUS FLUORIDE |
| Active Numerator Strength: | 1.8 |
| Active Ingredient Unit: | g/g |
| Pharm Classes: | |
| DEA Schedule: |