Product NDC: | 50227-1006 |
Proprietary Name: | Take Home Fluoride |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | 5 mg/g & nbsp; Sodium Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50227-1006 |
Labeler Name: | Patterson Dental Supply Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19970415 |
Package NDC: | 50227-1006-2 |
Package Description: | 1 TUBE in 1 BOX, UNIT-DOSE (50227-1006-2) > 56 g in 1 TUBE |
NDC Code | 50227-1006-2 |
Proprietary Name | Take Home Fluoride |
Package Description | 1 TUBE in 1 BOX, UNIT-DOSE (50227-1006-2) > 56 g in 1 TUBE |
Product NDC | 50227-1006 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 19970415 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Patterson Dental Supply Inc |
Substance Name | SODIUM FLUORIDE |
Strength Number | 5 |
Strength Unit | mg/g |
Pharmaceutical Classes |