Product NDC: | 55312-158 |
Proprietary Name: | Western Family Sensitive Whitening 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, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55312-158 |
Labeler Name: | Western Family Food, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20070502 |
Package NDC: | 55312-158-09 |
Package Description: | 113 g in 1 TUBE (55312-158-09) |
NDC Code | 55312-158-09 |
Proprietary Name | Western Family Sensitive Whitening Fluoride |
Package Description | 113 g in 1 TUBE (55312-158-09) |
Product NDC | 55312-158 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Potassium Nitrate and Sodium Fluoride |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20070502 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Western Family Food, Inc. |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | 5; 2.43 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |