Product NDC: | 64778-1379 |
Proprietary Name: | Denti-Care |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | .01; .0176 g/g; g/g & nbsp; Sodium Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64778-1379 |
Labeler Name: | AR Medicom Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20030501 |
Package NDC: | 64778-1379-1 |
Package Description: | 125 g in 1 BOTTLE, SPRAY (64778-1379-1) |
NDC Code | 64778-1379-1 |
Proprietary Name | Denti-Care |
Package Description | 125 g in 1 BOTTLE, SPRAY (64778-1379-1) |
Product NDC | 64778-1379 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | AEROSOL, FOAM |
Route Name | DENTAL |
Start Marketing Date | 20030501 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | AR Medicom Inc |
Substance Name | HYDROFLUORIC ACID; SODIUM FLUORIDE |
Strength Number | .01; .0176 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |