NOBLE 1 PLUS- xylitol powder, dentifrice

Noble 1 Plus by

Drug Labeling and Warnings

Noble 1 Plus by is a Otc medication manufactured, distributed, or labeled by Hankuk Bowonbio Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

INACTIVE INGREDIENT

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>

PURPOSE

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 CHILDREN

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

INDICATIONS & USAGE

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

WARNINGS

■ For tooth only.

■ Avoid contact with eyes.

■ Do not swallow. If swallowed, get medical help.
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DOSAGE & ADMINISTRATION

brush your teeth by putting appropriate amount of powder
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PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

NOBLE 1 PLUS 
xylitol powder, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60319-4001
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
XYLITOL (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E)	XYLITOL	0.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60319-4001-1	25 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/30/2012

Labeler - Hankuk Bowonbio Co., Ltd (690045133)

Registrant - Hankuk Bowonbio Co., Ltd (690045133)

Establishment
Name	Address	ID/FEI	Business Operations
Hankuk Bowonbio Co., Ltd		690045133	manufacture(60319-4001)