NOBLE 1 PLUS- xylitol powder, dentifrice 
Hankuk Bowonbio Co., Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

active ingredient: xylitol<text><contentstyleCode="xmChange"></content></text>

cetylpyridinium chloride, lactose monohydrate, corn starch, d-sorbitol, ubidecarenone, glycyrrhizae extract, tea chatechin, hydroxyapatite, propolis extract, menthol powder, spirulina color<text><contentstyleCode="xmChange"></content></text>

whiten and strong teeth

removal of bad breath

prevention of gingivitis and periodontitis

prevention of periodontal diseases and gum diseases

removal of dental plaque<text><contentstyleCode="xmChange"></content></text>

keep out of reach of the children<text><contentstyleCode="xmChange"></content></text>

apply Proper Amount of the toothpaste on the tooth.<text><contentstyleCode="xmChange"></content></text>

■ For tooth only.

■ Avoid contact with eyes.

■ Do not swallow. If swallowed, get medical help.
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brush your teeth by putting appropriate amount of powder
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package insert<text><contentstyleCode="xmChange"></content></text>

NOBLE 1 PLUS 
xylitol powder, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60319-4001
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
XYLITOL (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E) XYLITOL0.7 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
STARCH, CORN (UNII: O8232NY3SJ)  
SORBITOL (UNII: 506T60A25R)  
UBIDECARENONE (UNII: EJ27X76M46)  
LICORICE (UNII: 61ZBX54883)  
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:60319-4001-125 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/30/2012
Labeler - Hankuk Bowonbio Co., Ltd (690045133)
Registrant - Hankuk Bowonbio Co., Ltd (690045133)
Establishment
NameAddressID/FEIBusiness Operations
Hankuk Bowonbio Co., Ltd690045133manufacture(60319-4001)

Revised: 12/2019
Document Id: 98ee91f0-4a19-51dd-e053-2995a90a35a5
Set id: d6be484e-40e2-4b23-bed7-86845a96d709
Version: 2
Effective Time: 20191204
 
Hankuk Bowonbio Co., Ltd