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 |