WILLO BUBBLE TWIST- sodium fluoride paste, dentifrice

Willo Bubble Twist by

Drug Labeling and Warnings

Willo Bubble Twist by is a Otc medication manufactured, distributed, or labeled by Willo 32 Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Sodium Fluoride 0.22%

(0.10% w/v Fluoride Ion)

Purpose Section

Purpose

Anticavity

Use Section

Use

Aids in the prevention of dental cavities

Warnings

Keep out of reach of children under 6 years of age, without adult supervision. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 2 years of age and older:

  brush teeth thoroughly, preferably

  after each meal or at least twice a

  day, or as directed by a dentist or

  doctor

• children under 6 years of age:

  instruct in good brushing and

  rinsing habits (to minimize swallowing). Supervise as

  necessary until capable of using

  without supervision

• children under 2 years of age:

  consult a dentist or doctor.

Inactive Ingredients

Water, Sorbitol, Sodium Cocoyl Glutamate, Glycerin, PEG-400, Sucralose, Citric Acid, Flavor, Beta-Glucan, Sodium Bicarbonate, Sodium Benzoate, Stevioside, Sodium Ascorbyl Phosphate, Menthol, Calcium Citrate

Questions or comments?

Tel: 1(888) 509-0459 or Email: support@willo.com

Visit us at willo.com

Distributed by: Willo 32, Inc.

New York NY 10016

Willo.com

Flavor description

BUBBLEGUM FLAVOR

Free of claims

Dye free

SLS free

Sulfate free

Paraben free

Gluten free

Distributor name and address

Dist. by: Willo 32, Inc

New York, NY 10006

1 (888) 509-0459

Broken seal warning

Do not use if

seal under cap

is broken or missing.

Willo Bubble Twist 8 oz Label

Willo

Bubble Twist

Anticavity Fluoride Liquid Toothpaste

Helps Prevent Cavities

& Strengthens Enamel

8 fl oz (237 ml)

Label images

INGREDIENTS AND APPEARANCE

WILLO BUBBLE TWIST 
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84185-102
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
CALCIUM CITRATE (UNII: MLM29U2X85)
STEVIOSIDE (UNII: 0YON5MXJ9P)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
WATER (UNII: 059QF0KO0R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
YEAST .BETA.-D-GLUCAN (UNII: 44FQ49X6UN)
MENTHOL (UNII: L7T10EIP3A)
CITRIC ACID (UNII: 2968PHW8QP)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
PEG-400 (UNII: 2AS3MDK9CB)

Product Characteristics
Color		Score
Shape		Size
Flavor	BUBBLE GUM	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84185-102-08	237 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/10/2025
2	NDC: 84185-102-22	2 in 1 BOX	09/10/2025
2	NDC: 84185-102-02	59 mL in 1 BOTTLE, PUMP; 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	09/10/2025

Labeler - Willo 32 Inc (105977106)