| Product NDC: | 55504-4341 |
| Proprietary Name: | dawnmist |
| Non Proprietary Name: | sodium fluoride |
| Active Ingredient(s): | 39.9 g/181.4g & nbsp; sodium fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55504-4341 |
| Labeler Name: | Donavan |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111101 |
| Package NDC: | 55504-4341-8 |
| Package Description: | 181.4 g in 1 TUBE (55504-4341-8) |
| NDC Code | 55504-4341-8 |
| Proprietary Name | dawnmist |
| Package Description | 181.4 g in 1 TUBE (55504-4341-8) |
| Product NDC | 55504-4341 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium fluoride |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Donavan |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 39.9 |
| Strength Unit | g/181.4g |
| Pharmaceutical Classes |