| Product NDC: | 53045-252 |
| 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: | 53045-252 |
| Labeler Name: | Dharma Research, inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130422 |
| Package NDC: | 53045-252-44 |
| Package Description: | 126 g in 1 BOTTLE (53045-252-44) |
| NDC Code | 53045-252-44 |
| Proprietary Name | Ionite APF |
| Package Description | 126 g in 1 BOTTLE (53045-252-44) |
| Product NDC | 53045-252 |
| 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 |