| Product NDC: | 76328-222 |
| Proprietary Name: | EcoDent Res-Q-Dent |
| Non Proprietary Name: | Potassium Nitrate |
| Active Ingredient(s): | 50 mg/g & nbsp; Potassium Nitrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76328-222 |
| Labeler Name: | Lotus Brands, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130601 |
| Package NDC: | 76328-222-01 |
| Package Description: | 1 TUBE in 1 CARTON (76328-222-01) > 85 g in 1 TUBE |
| NDC Code | 76328-222-01 |
| Proprietary Name | EcoDent Res-Q-Dent |
| Package Description | 1 TUBE in 1 CARTON (76328-222-01) > 85 g in 1 TUBE |
| Product NDC | 76328-222 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Potassium Nitrate |
| Dosage Form Name | PASTE |
| Route Name | ORAL |
| Start Marketing Date | 20130601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Lotus Brands, Inc. |
| Substance Name | POTASSIUM NITRATE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |