Product NDC: | 68747-6032 |
Proprietary Name: | Iodent Fluoride Mint |
Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
Active Ingredient(s): | 7.6 mg/g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68747-6032 |
Labeler Name: | Dabur India Limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120228 |
Package NDC: | 68747-6032-1 |
Package Description: | 1 TUBE in 1 CARTON (68747-6032-1) > 181 g in 1 TUBE |
NDC Code | 68747-6032-1 |
Proprietary Name | Iodent Fluoride Mint |
Package Description | 1 TUBE in 1 CARTON (68747-6032-1) > 181 g in 1 TUBE |
Product NDC | 68747-6032 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20120228 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dabur India Limited |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | 7.6 |
Strength Unit | mg/g |
Pharmaceutical Classes |