Product NDC: | 57353-101 |
Proprietary Name: | POWER WHITE 7 |
Non Proprietary Name: | SODIUM FLUORIDE POTASSIUM NITRATE |
Active Ingredient(s): | 5; .24 g/100g; g/100g & nbsp; SODIUM FLUORIDE POTASSIUM NITRATE |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57353-101 |
Labeler Name: | DENTOVATIONS INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121201 |
Package NDC: | 57353-101-53 |
Package Description: | 1 TUBE in 1 BOX (57353-101-53) > 74 g in 1 TUBE (57353-101-13) |
NDC Code | 57353-101-53 |
Proprietary Name | POWER WHITE 7 |
Package Description | 1 TUBE in 1 BOX (57353-101-53) > 74 g in 1 TUBE (57353-101-13) |
Product NDC | 57353-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM FLUORIDE POTASSIUM NITRATE |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20121201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | DENTOVATIONS INC |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | 5; .24 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |