Home
>
National Drug Code (NDC)
>
Sensitive Whitening
Sensitive Whitening - 59779-814-58 - (Fluoride and Potassium Nitrate)
Drug Information of Sensitive Whitening
| Product NDC: | 59779-814 |
| Proprietary Name: | Sensitive Whitening |
| Non Proprietary Name: | Fluoride and Potassium Nitrate |
| Active Ingredient(s): | 5; .15 g/100g; g/100g & nbsp; Fluoride and Potassium Nitrate |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sensitive Whitening
| Product NDC: | 59779-814 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111213 |
Package Information of Sensitive Whitening
| Package NDC: | 59779-814-58 |
| Package Description: | 12 CAN in 1 CASE (59779-814-58) > 121.6 g in 1 CAN (59779-814-57) |
NDC Information of Sensitive Whitening
| NDC Code | 59779-814-58 |
| Proprietary Name | Sensitive Whitening |
| Package Description | 12 CAN in 1 CASE (59779-814-58) > 121.6 g in 1 CAN (59779-814-57) |
| Product NDC | 59779-814 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Fluoride and Potassium Nitrate |
| Dosage Form Name | GEL |
| Route Name | DENTAL |
| Start Marketing Date | 20111213 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CVS Pharmacy |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 5; .15 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
