| Product NDC: | 45163-451 |
| Proprietary Name: | NANO SILVER TOOTHPASTE |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE, SILICON DIOXIDE, GLYCERIN |
| Active Ingredient(s): | 5; 14; 1.4 g/200g; g/200g; g/200g & nbsp; SODIUM MONOFLUOROPHOSPHATE, SILICON DIOXIDE, GLYCERIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 45163-451 |
| Labeler Name: | Nanowell Korea Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100120 |
| Package NDC: | 45163-451-63 |
| Package Description: | 200 g in 1 TUBE (45163-451-63) |
| NDC Code | 45163-451-63 |
| Proprietary Name | NANO SILVER TOOTHPASTE |
| Package Description | 200 g in 1 TUBE (45163-451-63) |
| Product NDC | 45163-451 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE, SILICON DIOXIDE, GLYCERIN |
| Dosage Form Name | PASTE |
| Route Name | ORAL |
| Start Marketing Date | 20100120 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Nanowell Korea Inc |
| Substance Name | GLYCERIN; SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 5; 14; 1.4 |
| Strength Unit | g/200g; g/200g; g/200g |
| Pharmaceutical Classes |