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 |