Product NDC: | 53045-251 |
Proprietary Name: | Ionite APF |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | 1.5498 g/126g & nbsp; Sodium Fluoride |
Administration Route(s): | DENTAL; ORAL; TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53045-251 |
Labeler Name: | Dharma Research, inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130422 |
Package NDC: | 53045-251-44 |
Package Description: | 126 g in 1 BOTTLE (53045-251-44) |
NDC Code | 53045-251-44 |
Proprietary Name | Ionite APF |
Package Description | 126 g in 1 BOTTLE (53045-251-44) |
Product NDC | 53045-251 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | AEROSOL, FOAM |
Route Name | DENTAL; ORAL; TOPICAL |
Start Marketing Date | 20130422 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Dharma Research, inc. |
Substance Name | SODIUM FLUORIDE |
Strength Number | 1.5498 |
Strength Unit | g/126g |
Pharmaceutical Classes |