Dr.NOAH MARUTOOTHPASTE by DONG IL PHARMS CO., LTD.

Dr.NOAH MARUTOOTHPASTE by

Drug Labeling and Warnings

Dr.NOAH MARUTOOTHPASTE by is a Otc medication manufactured, distributed, or labeled by DONG IL PHARMS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR.NOAH MARUTOOTHPASTE- precipitated calcium carbonate paste 
DONG IL PHARMS 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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ACTIVE INGREDIENT

precipitated calcium carbonate

INACTIVE INGREDIENT

d-sorbitol solution, water, concentrated glycerin, scutellaria bak, alensls root extract, xanthan gurn, sodium cocoyl glutamate, sodium
cocoyl isethionate, 1-mentho~ steviol, glycoside, xylitol, mentha pulagium, oil, peppermint oil, spearmint oil, sodium chloride, silicon dioxide

PURPOSE

■ Keeps teeth white and strong

■ Keep the oral cavity clean

■ Prevents tooth decay and bad breath caused by fluoride

■ Removing plaque, preventing gingivitis and periodontitis

■ Periodontal Disease Prevention

■ Gum Disease Prevention

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WARNING

For oral use only
When using this product

■ This toothpaste has a 1,000 ppm fluoride content

■ Do not use other than brushing teeth and be careful not to swallow

Keep out of reach of children

■ if swallowed, seek medical help or contact the poison control center immediately

USES

for oral use only

INDICATION & USAGE SECTION

Brush thoroughly ofter each meal or at least twice a day, as directed by yourdoctorordendst
Do not swallow.

Do not use if seal is broken or missing.

store in a cool, dry place.

label

DR.NOAH MARUTOOTHPASTE 
precipitated calcium carbonate paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73242-0111
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION0.22 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SORBITOL (UNII: 506T60A25R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73242-0111-1120 g in 1 TUBE; Type 0: Not a Combination Product09/17/202110/29/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/17/202110/29/2021
Labeler - DONG IL PHARMS CO., LTD. (557810721)
Registrant - DONG IL PHARMS CO., LTD. (557810721)
Establishment
NameAddressID/FEIBusiness Operations
DONG IL PHARMS CO., LTD.557810721manufacture(73242-0111)

Revised: 10/2021