DENTI WHOO CTS GUM CARETOOTHPASTE- silicon dioxide, sodium fluoride, tocopherol acetate paste, dentifrice

Denti Whoo CTS Gum CareToothpaste by

Drug Labeling and Warnings

Denti Whoo CTS Gum CareToothpaste by is a Otc medication manufactured, distributed, or labeled by SUN LIFE SCIENCE CO LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Silicon Dioxide, Sodium Fluoride, Tocopherol Acetate

INACTIVE INGREDIENT

Chitosan, Propolis Extract,Xylitol, L-Menthol, Glycyrrhiza Extract, Rosemary Extract, Green Tea Extract, AloeExtract, Sage Extract, Matricaria Extract, Sodium Bicarbonate, Peppermint Oil, SodiumCocoyl Glutamate, D-Sorbitol Solution, Concentrated Glycerin, SodiumCarboxymethylcellulose, Water

PURPOSE

(1) Keep your teeth white and strong.(2) Keep your mouth clean.(3) Refresh the inside of the mouth.(4) Prevent tooth decay and remove bad breath due to fluorine.(5) Increase the esthetic effect.(6) Prevention of gingivitis and periodontitis(alveolar fistula)(7) Prevention of periodontal disease and gum disease(8) Plaque removal(anti-plaque)

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

Brushing the teeth with a suitable amount

WARNINGS

(1) The fluoride content of this toothpaste is 1,000 ppm.(2) Do not swallow and rinse mouth thoroughly after use(3) If you experience any problems with your gums or mouth during use,discontinue use and consult your doctor(4) For children under 6 years of age, use small amounts of toothpaste. And use itunder the supervision of a guardian to avoid sucking or swallowing(5) Consult a physician or dentist immediately if a child under 6 years old hasswallowed large quantities(6) Keep out of the reach of children under 6 years of age

DOSAGE & ADMINISTRATION

For dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DENTI WHOO CTS GUM CARETOOTHPASTE 
silicon dioxide, sodium fluoride, tocopherol acetate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 86157-0013
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.22 g  in 100 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	15 g  in 100 g
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1)	.ALPHA.-TOCOPHEROL ACETATE	0.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
WATER (UNII: 059QF0KO0R)
LEVOMENTHOL (UNII: BZ1R15MTK7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86157-0013-1	50 g in 1 TUBE; Type 0: Not a Combination Product	04/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/06/2022

Labeler - SUN LIFE SCIENCE CO LTD (695149648)

Registrant - SUN LIFE SCIENCE CO LTD (695149648)

Establishment
Name	Address	ID/FEI	Business Operations
SUN LIFE SCIENCE CO LTD		695149648	manufacture(86157-0013)