GREENSALTRAIN TOOTH- precipitated calcium carbonate, dibasic calcium phosphate, aminocaproic acid, aluminium chlorohydroxy allantoinate paste, dentifrice 
K.Boeun Pharmaceutical 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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Silicon Dioxide, Aluminium Chlorohydroxy Allantoinate, Aminocaproic Acid

D-Sorbitol Solution
Concentrated Glycerin
Polyethylene Glycol 1500
Carboxymethylcellulose Sodium
Sodium Cocoyl Glutamate
Xylitol
Enzymatically Modified Stevia

Sodium Chloride
Tocopherol Acetate
Ascorbic Acid

l-Menthol
Mentha Oil

Bifidus Extract
Green Tea Extract

Aloe Extract

Sage Extract

Matricaria Extract

Eucalyptus Extract
Centella extract
Water

For dental care

Keep out of reach of children

Apply an appropriate amount to your toothbrush and brush your teeth by brushing.

Warnings

Keep out of reach of children

■ If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Other Information

■ Store in an airtight container at room temperature

■ Date of use : 36 months from the date of manufacture

For dental use only

1

GREENSALTRAIN TOOTH 
precipitated calcium carbonate, dibasic calcium phosphate, aminocaproic acid, aluminium chlorohydroxy allantoinate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74724-0026
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCLOXA (UNII: 18B8O9DQA2) (ALCLOXA - UNII:18B8O9DQA2) ALCLOXA0.05 g  in 100 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE13.5 g  in 100 g
AMINOCAPROIC ACID (UNII: U6F3787206) (AMINOCAPROIC ACID - UNII:U6F3787206) AMINOCAPROIC ACID0.05 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
XYLITOL (UNII: VCQ006KQ1E)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74724-0026-1100 g in 1 TUBE; Type 0: Not a Combination Product05/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/01/2021
Labeler - K.Boeun Pharmaceutical Co.,Ltd. (695674074)
Registrant - K.Boeun Pharmaceutical Co.,Ltd. (695674074)
Establishment
NameAddressID/FEIBusiness Operations
K.Boeun Pharmaceutical Co.,Ltd.695674074manufacture(74724-0026)

Revised: 5/2021
Document Id: c3232d0d-a662-8c60-e053-2a95a90ad46b
Set id: c3232d90-ea65-304d-e053-2995a90a7b09
Version: 1
Effective Time: 20210525
 
K.Boeun Pharmaceutical Co.,Ltd.