| Product NDC: | 60319-4001 |
| Proprietary Name: | Noble 1 Plus |
| Non Proprietary Name: | XYLITOL |
| Active Ingredient(s): | .7 g/100g & nbsp; XYLITOL |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | POWDER, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 60319-4001 |
| Labeler Name: | Hankuk Bowonbio Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20121130 |
| Package NDC: | 60319-4001-1 |
| Package Description: | 25 g in 1 BOTTLE, PLASTIC (60319-4001-1) |
| NDC Code | 60319-4001-1 |
| Proprietary Name | Noble 1 Plus |
| Package Description | 25 g in 1 BOTTLE, PLASTIC (60319-4001-1) |
| Product NDC | 60319-4001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | XYLITOL |
| Dosage Form Name | POWDER, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20121130 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Hankuk Bowonbio Co., Ltd |
| Substance Name | XYLITOL |
| Strength Number | .7 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |