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 |