| 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: | 68599-0123-2 |
| Package Description: | 144 BOX in 1 CARTON (68599-0123-2) > 1 TUBE in 1 BOX > 78 g in 1 TUBE |
| NDC Code | 68599-0123-2 |
| Proprietary Name | McKesson Fluoride |
| Package Description | 144 BOX in 1 CARTON (68599-0123-2) > 1 TUBE in 1 BOX > 78 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 |