Product NDC: | 68599-0123 |
Proprietary Name: | McKesson Fluoride |
Non Proprietary Name: | Sodium Monofluorophosphate |
Active Ingredient(s): | 2.43 mg/g & nbsp; Sodium Monofluorophosphate |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68599-0123 |
Labeler Name: | McKesson Medical-Surgical |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120217 |
Package NDC: | 68599-0123-1 |
Package Description: | 144 BOX in 1 CARTON (68599-0123-1) > 1 TUBE in 1 BOX > 43 g in 1 TUBE |
NDC Code | 68599-0123-1 |
Proprietary Name | McKesson Fluoride |
Package Description | 144 BOX in 1 CARTON (68599-0123-1) > 1 TUBE in 1 BOX > 43 g in 1 TUBE |
Product NDC | 68599-0123 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Monofluorophosphate |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20120217 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McKesson Medical-Surgical |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | 2.43 |
Strength Unit | mg/g |
Pharmaceutical Classes |