CLEAN BREATH 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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Precipitated Calcium Carbonate, Dibasic Calcium Phosphate, Aminocaproic Acid, Aluminium Chlorohydroxy Allantoinate

Water, D-Sorbitol Solution, Concentrated Glycerin, Silicon Dioxide, Sodium Cocoyl Glutamate, Polyethylene Glycol 1500, Xanthangum, Mentha Oil, Enzymatically Modified Stevia, Titanium Oxide, Sodium Chloride, Propolis Extract, l-Menthol, Xylitol, Ascorbic Acid, Green Tea Extract, Aloe Extract, Tocopherol Acetate

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

label

CLEAN BREATH TOOTH 
precipitated calcium carbonate, dibasic calcium phosphate, aminocaproic acid, aluminium chlorohydroxy allantoinate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74724-0028
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J) (CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS - UNII:L11K75P92J) CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS0.07 g  in 100 g
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE36 g  in 100 g
ALCLOXA (UNII: 18B8O9DQA2) (ALCLOXA - UNII:18B8O9DQA2) ALCLOXA0.06 g  in 100 g
AMINOCAPROIC ACID (UNII: U6F3787206) (AMINOCAPROIC ACID - UNII:U6F3787206) AMINOCAPROIC ACID0.06 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
XYLITOL (UNII: VCQ006KQ1E)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74724-0028-1180 g in 1 TUBE; Type 0: Not a Combination Product11/30/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/30/2021
Labeler - K.Boeun Pharmaceutical Co.,Ltd. (695674074)
Registrant - K.Boeun Pharmaceutical Co.,Ltd. (695674074)
Establishment
NameAddressID/FEIBusiness Operations
K.Boeun Pharmaceutical Co.,Ltd.695674074manufacture(74724-0028)

Revised: 11/2021
Document Id: d1feeb95-7f4c-c8de-e053-2995a90aea5e
Set id: d1feebb0-c685-25e0-e053-2995a90ac5ea
Version: 1
Effective Time: 20211130
 
K.Boeun Pharmaceutical Co.,Ltd.