BRUSH BUDDIES - HOT WHEELS ANTICAVITY FLUORIDE- sodium fluoride paste, dentifrice

Brush Buddies - Hot Wheels ANTICAVITY FLUORIDE by

Drug Labeling and Warnings

Brush Buddies - Hot Wheels ANTICAVITY FLUORIDE by is a Otc medication manufactured, distributed, or labeled by Ashtel Studios Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Sodium fluoride 0.243%
(1100 ppm Fluoride ion)

Purpose

Anticavity

Uses

helps protect teeth and roots against cavities.

Warnings

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

Directions

Adults and children 2 years and older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist.
Do not swallow.
Children 2 to 6 years: to minimize swallowing use a pea-sized amount and supervise children's brushing and rinsing until good habits are established.
Children under 2 years of age: Consult a dentist or doctor.

Inactive ingredients

Sorbitol, Silica, Aqua, PEG-32, Xylitol, Sodium Lauryl Sulfate, Flavor, Cellulose Gum, Benzyl Alcohol, Sodium Benzoate, Sodium Saccharin, Trisodium Phosphate, D & C Red # 33, FD & C Yellow # 5

Questions or comments?

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

HELPS PREVENT CAVITIES

STRAWBERRY FLAVOR

make brushing fun!®

CAUTION:
AVOID EXCESSIVE INGESTION.
NOT FOR PETS.
NOT TESTED ON ANIMALS.

MATTEL
HOT WHEELS™ and associated trademarks and trade dress are owned by, and used under license from, Mattel.
©2024 Mattel.

DESIGNED IN U.S.A MADE IN INDIA

Brush Buddies®
WWW.BRUSHBUDDIES.COM

1-909-434-0911 INTERNATIONAL

PATENTS, COPYRIGHTS & TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY ASHTEL STUDIOS INC.
ONTARIO, CALIFORNIA 91761

Packaging

INGREDIENTS AND APPEARANCE

BRUSH BUDDIES - HOT WHEELS ANTICAVITY FLUORIDE 
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-083
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.243 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)
XYLITOL (UNII: VCQ006KQ1E)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Characteristics
Color	pink	Score
Shape		Size
Flavor	STRAWBERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70108-083-01	1 in 1 BOX	05/29/2024
1		113 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	05/29/2024

Labeler - Ashtel Studios Inc. (148689180)