NOBLE G PLUS - xylitol paste, 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

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

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 the children

apply Proper Amount of the toothpaste on the tooth.

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

brush your teeth by putting appropriate amount of tooth paste

package insert
NOBLE G PLUS 
xylitol paste, dentifrice
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:60319-3001
Route of Administration DENTAL DEA Schedule     
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
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)

Revised: 11/2012
Document Id: 54d953fc-a218-4108-8119-5fc5a18aa5f9
Set id: 0392a152-ee0d-4f9d-a85f-02170473d6eb
Version: 1
Effective Time: 20121130
 
Hankuk Bowonbio Co., Ltd