SALTRAIN LTOOTHPASTE- sodium chloride, precipitated calcium carbonate 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.

----------

Sodium Chloride, Precipitated Calcium Carbonate

D-Sorbitol Solution
Concentrated Glycerin
Polyethylene Glycol 1500
Xanthan gum
Titanium Oxide
Silicon Dioxide
Sodium Cocoyl Glutamate
Enzymatically Modified Stevia
Xylitol
Ascorbic Acid
Tocopherol Acetate
Propolis Extract
Green Tea Extract

Aloe Extract
l-Menthol
Mentha Oil
Lemon Oil
Water

aids in the prevention of dental cavities

plaque removal (anti-plaque)

prevention of periodontal disease, prevention of gum disease

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

SALTRAIN LTOOTHPASTE 
sodium chloride, precipitated calcium carbonate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74724-0031
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE3 g  in 100 g
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE33 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
XYLITOL (UNII: VCQ006KQ1E)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74724-0031-1180 g in 1 TUBE; Type 0: Not a Combination Product01/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/01/2023
Labeler - K.Boeun Pharmaceutical Co.,Ltd. (695674074)
Registrant - K.Boeun Pharmaceutical Co.,Ltd. (695674074)
Establishment
NameAddressID/FEIBusiness Operations
K.Boeun Pharmaceutical Co.,Ltd.695674074manufacture(74724-0031)

Revised: 12/2022
Document Id: f126e30f-5f3a-7bf9-e053-2a95a90a265d
Set id: f126df43-b31a-13c2-e053-2a95a90a523c
Version: 1
Effective Time: 20221231
 
K.Boeun Pharmaceutical Co.,Ltd.