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 |