DR.NOAH MARUFTOOTHPASTE- sodium monofluorophosphate paste

Dr.NOAH MARUFTOOTHPASTE by

Drug Labeling and Warnings

Dr.NOAH MARUFTOOTHPASTE 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

Sodium Fluoride

INACTIVE INGREDIENT

Precipitated Calcium Carbonate
Xanthangum
Sodium Chloride
Steviol Glycoside
Xylitol
D-Sorbitol Solution
Concentrated Glycerin
Sodium Cocoyl Glutamate
Sodium Cocoyl Isethionate
Bioactive Herb Complex-C
L-Menthol
Menthol Pulegium Oil
Peppermint Oil
Spearmint Oil
Sage Extract
Aloe Extract
Green Tea Extract
Water

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 MARUFTOOTHPASTE 
sodium monofluorophosphate paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82359-0001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.22 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SORBITOL (UNII: 506T60A25R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82359-0001-1	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
OTC monograph final	part355	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(82359-0001)

Establishment
Name	Address	ID/FEI	Business Operations
DR.Noah		695333875	api manufacture(82359-0001)