DENTI WHOO CTS GERM FREE-F- sodium fluoride liquid

DENTI WHOO CTS GERM FREE-F by

Drug Labeling and Warnings

DENTI WHOO CTS GERM FREE-F 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

Sodium Fluoride

INACTIVE INGREDIENT

Sodium Fluoride
Citric Acid
Sodium Citrate
Stevioside
Xylitol
Chitosan
Citrus paradisi(Grapefruit) Fruit extract
Saponaria Officinalis Extract
hamomilla Recutita (Matricaria) Leaf Extra
Mentol
Fragnance
Glycerin
Water

PURPOSE

Tooth-decay prevention, Odor removal from the mouth

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

Put about 10 to 15ml in your mouth, gargle for about 30 seconds, and spit it out.

WARNINGS

1.General Attention
1) Please observe the prescribed usage and capacity.
2) Do not use it for children under the age of six.
3) Use it under the supervision of guardian when using it for children over the age of seven.
4) This product contains fluorine, so if you drink it incorrectly, consult your doctor or pharmacist.
2. Storage Precautions
1) Keep out of reach of children.
2) Avoid direct sunlight and store in a cool place as much as possible.
3) Do not replace it in other containers to prevent misuse and to preserve quality.

DOSAGE & ADMINISTRATION

For dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DENTI WHOO CTS GERM FREE-F 
sodium fluoride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 86157-0012
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
XYLITOL (UNII: VCQ006KQ1E)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86157-0012-1	250 mL in 1 BOTTLE; 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(86157-0012)