AUTOBRUSH BUBBLEGUM- sodium fluoride liquid

AutoBrush Bubblegum by

Drug Labeling and Warnings

AutoBrush Bubblegum by is a Otc medication manufactured, distributed, or labeled by Lander Enterprises, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Sodium Fluoride 0.24%

Purpose

Anticavity

Uses

Aids in the prevention of dental cavities.

Warnings

Keep out of reach of children under 6 years of age. If more than used for brushing
is accidentally swallowed, get medical help or contact a Poison Control Central right away.

KEEP OUT OF REACH OF CHILDREN

Directions

● Adults and children 2 years of age and older: Brush teeth thoroughly, preferably
after each meal or at least twice per day, or as directed by a dentist or physician.
● Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing).
● Shake before use.
● Squirt two times into your mouth and start brushing.
● Supervise children as necessary until capable of using without supervision.
● Children under 2 years of age: consult a dentist or physician.

Inactive Ingredients

Aqua, Glycerin, Sorbitol, Poloxamer, Xylitol, Natural Bubblegum Flavor, Nano Silver, Potassium Sorbate, Stevioside, Citric Acid, Calcium Citrate

● Questions?

• Email Support: customercare@autobrush.com

●   Phone Support: 1-888-468-7404

Product label

INGREDIENTS AND APPEARANCE

AUTOBRUSH BUBBLEGUM 
sodium fluoride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82913-001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.24 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SORBITOL (UNII: 506T60A25R)
POLOXAMER 407 (UNII: TUF2IVW3M2)
XYLITOL (UNII: VCQ006KQ1E)
SILVER (UNII: 3M4G523W1G)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
STEVIOSIDE (UNII: 0YON5MXJ9P)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CALCIUM CITRATE (UNII: MLM29U2X85)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82913-001-01	1 in 1 CARTON	08/01/2022
1		50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	08/01/2022

Labeler - Lander Enterprises, LLC (068619221)