| 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 |