NOBLE G PLUS- xylitol paste, dentifrice

Noble G Plus by

Drug Labeling and Warnings

Noble G 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

INACTIVE INGREDIENT

silicone dioxide, sodium monofluorophosphate, hydrated silicone dioxide, d-sorbitol, carboxymethylcellulose sodium, sodium lauryl sulfate, sodium saccharin, gold leaf, green tea extract, polyethylene glycol 1500, L-menthol, hydroxyapatite, chitosan, stearic acid, polysorbate 80, water

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

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

apply Proper Amount of the toothpaste on the tooth.

WARNINGS

■ For tooth only.
■ Avoid contact with eyes.
■ Do not swallow. If swallowed, get medical help.

DOSAGE & ADMINISTRATION

brush your teeth by putting appropriate amount of tooth paste

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NOBLE G PLUS 
xylitol paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60319-3001
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
WATER (UNII: 059QF0KO0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SORBITOL (UNII: 506T60A25R)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602)
GOLD (UNII: 79Y1949PYO)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
LEVOMENTHOL (UNII: BZ1R15MTK7)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
CHITOSAN OLIGOSACCHARIDE (UNII: 23R93M6Y64)
ISOSTEARIC ACID (UNII: X33R8U0062)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60319-3001-1	130 g in 1 TUBE; Type 0: Not a Combination Product	12/06/2019

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(60319-3001)