DR.NOAH MARUTOOTHPASTE- precipitated calcium carbonate paste

Dr.NOAH MARUTOOTHPASTE by

Drug Labeling and Warnings

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

Drug Details [pdf]

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.NOAH MARUTOOTHPASTE 
precipitated calcium carbonate paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82359-0002
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	0.22 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SORBITOL (UNII: 506T60A25R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82359-0002-1	120 g in 1 TUBE; Type 0: Not a Combination Product	10/29/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/29/2021

Labeler - DR.Noah (695333875)

Registrant - DR.Noah (695333875)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(82359-0002)

Establishment
Name	Address	ID/FEI	Business Operations
DR.Noah		695333875	label(82359-0002)