BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY- sodium fluoride liquid

BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY by

Drug Labeling and Warnings

BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY by is a Otc medication manufactured, distributed, or labeled by Kingkey MBC Life Technology Group co., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

SODIUM FLUORIDE 0.03%

Purpose

Anticavity

Uses

helps protect teeth against cavities

Warnings

Keep out of reach of children under 6 years of age. lf you accidentally swallow more than used for rinsing, seek professional help or contact a Poison Control Center immediately.

KEEP OUT OF REACH OF CHILDREN

Directions

Adults and children 6 years and older:

• Use daily after you brush your teeth with toothpaste
• Rinse toothpaste from mouth prior to use.
• Shake well before each use.Twist and remove cap.
• Rinse or gargle for 30 seconds with 15 ml and spit out.
• Do Notswallow the rinse.
• Do Noteat or drink for 30 minutes after rinsing
• Supervise children as necessary.
• Children under 6 years of age, consult with a dentist or doctor.

Inactive ingredients

Water, SORBITOL, GLYCERIN, XYLITOL, POTASSIUM SORBATE, SODIUM BENZOATE, PEG-40 HYDROGENATED CASTOR OIL, FLAVOR
SODIUM FLUORIDE, SODIUM SACCHARIN, CETYLPYRIDINIUM CHLORIDE, SUCRALOSE, CITRIC ACID, METHYL DIISOPROPYL PROPIONAMIDE
D&C Red No.33（CI 17200, FD&C RED NO. 40

Questions or comments?

Call toll free 1-877-274-8358

Product label

INGREDIENTS AND APPEARANCE

BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY 
sodium fluoride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73928-021
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.03 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
XYLITOL (UNII: VCQ006KQ1E)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
SUCRALOSE (UNII: 96K6UQ3ZD4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73928-021-01	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/10/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	05/10/2024

Labeler - Kingkey MBC Life Technology Group co., LTD. (545349263)