Product NDC: | 11822-0002 |
Proprietary Name: | Rite Aid Sensitive Mint |
Non Proprietary Name: | Potassium Nirtate and Sodium Fluoride |
Active Ingredient(s): | 5; 2.43 mg/g; mg/g & nbsp; Potassium Nirtate and Sodium Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-0002 |
Labeler Name: | Rite Aid |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100719 |
Package NDC: | 11822-0002-1 |
Package Description: | 170 g in 1 CARTON (11822-0002-1) |
NDC Code | 11822-0002-1 |
Proprietary Name | Rite Aid Sensitive Mint |
Package Description | 170 g in 1 CARTON (11822-0002-1) |
Product NDC | 11822-0002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Potassium Nirtate and Sodium Fluoride |
Dosage Form Name | PASTE |
Route Name | DENTAL |
Start Marketing Date | 20100719 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Rite Aid |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | 5; 2.43 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |