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Dawnmist Fluoride
Dawnmist Fluoride - 65517-1000-0 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of Dawnmist Fluoride
| Product NDC: | 65517-1000 |
| Proprietary Name: | Dawnmist Fluoride |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .76 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dawnmist Fluoride
| Product NDC: | 65517-1000 |
| Labeler Name: | Dukal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120924 |
Package Information of Dawnmist Fluoride
| Package NDC: | 65517-1000-0 |
| Package Description: | 17 g in 1 TUBE (65517-1000-0) |
NDC Information of Dawnmist Fluoride
| NDC Code | 65517-1000-0 |
| Proprietary Name | Dawnmist Fluoride |
| Package Description | 17 g in 1 TUBE (65517-1000-0) |
| Product NDC | 65517-1000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20120924 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dukal Corporation |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .76 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
