| 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 |