Product NDC: | 0363-0631 |
Proprietary Name: | Walgreens Maximum Strength Sensitive Fluoride |
Non Proprietary Name: | Potassium Nitrate and Sodium Fluoride |
Active Ingredient(s): | 5; 2.43 mg/g; mg/g & nbsp; Potassium Nitrate and Sodium Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-0631 |
Labeler Name: | Walgreens |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20060606 |
Package NDC: | 0363-0631-09 |
Package Description: | 113 g in 1 TUBE (0363-0631-09) |
NDC Code | 0363-0631-09 |
Proprietary Name | Walgreens Maximum Strength Sensitive Fluoride |
Package Description | 113 g in 1 TUBE (0363-0631-09) |
Product NDC | 0363-0631 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Potassium Nitrate and Sodium Fluoride |
Dosage Form Name | PASTE |
Route Name | DENTAL |
Start Marketing Date | 20060606 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Walgreens |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | 5; 2.43 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |