| 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 |