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ControlRx Multi
ControlRx Multi - 48878-3110-6 - (sodium fluoride)
Drug Information of ControlRx Multi
| Product NDC: | 48878-3110 |
| Proprietary Name: | ControlRx Multi |
| Non Proprietary Name: | sodium fluoride |
| Active Ingredient(s): | 11 mg/g & nbsp; sodium fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ControlRx Multi
| Product NDC: | 48878-3110 |
| Labeler Name: | 3M ESPE Dental Products |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070801 |
Package Information of ControlRx Multi
| Package NDC: | 48878-3110-6 |
| Package Description: | 1 TUBE in 1 BOX (48878-3110-6) > 57 g in 1 TUBE |
NDC Information of ControlRx Multi
| NDC Code | 48878-3110-6 |
| Proprietary Name | ControlRx Multi |
| Package Description | 1 TUBE in 1 BOX (48878-3110-6) > 57 g in 1 TUBE |
| Product NDC | 48878-3110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sodium fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | ORAL |
| Start Marketing Date | 20070801 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | 3M ESPE Dental Products |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 11 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
