FDA.reportPublic FDA data

AutoBrush Mint

Manufacturer
Lander Enterprises, LLC
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:30:20

Label at a glance#

ProductAutoBrush Mint
Active ingredientSODIUM FLUORIDE
Label structure8 sections

Indications and uses

Aids in the prevention of dental cavities.

Dosage and administration

● 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 super...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.24%

Purpose

OTC - PURPOSE SECTION

Anticavity

Uses

INDICATIONS & USAGE SECTION

Aids in the prevention of dental cavities.

Warnings

WARNINGS SECTION

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.

Directions

DOSAGE & ADMINISTRATION SECTION

● 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

INACTIVE INGREDIENT SECTION

Aqua, Xylitol, Alkyl Glucoside, Peg-40 Hydrogenated Caster Oil, Stevia Rebaudiana Extract, LS 95, PVP-K30, Peppermint Flavor, Nano Silver,
Calcium Citrate, Potassium Sorbate, Citric Acid

● Questions?

SPL UNCLASSIFIED SECTION

  • Email Support: customercare@autobrush.com

●   Phone Support: 1-888-468-7404

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeqr.tryautobrush.com/g/3YDrTTiw3jqImage_004_2.jpg, Image_004_1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82913-004-01AutoBrush Mint1 in 1 CARTONLIQUID15
82913-004-01AutoBrush Mint50 mL in 1 BOTTLE, PLASTICLIQUID505

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82913-00482913-004-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
XYLITOLVCQ006KQ1EIACT
C12-20 ALKYL GLUCOSIDEK67N5Z1RUAIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT
SODIUM LAUROYL SARCOSINATE632GS99618IACT
POVIDONE K30U725QWY32XIACT
SILVER3M4G523W1GIACT
CALCIUM CITRATEMLM29U2X85IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM FLUORIDE8ZYQ1474W7ACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AutoBrush MintSODIUM FLUORIDELander Enterprises, LLC6bcd35f5-18ea-4fc8-84cd-06db73f38a1e2025-12-31WarningsExact identifier
ndc (package): 82913-004-01
ndc (product): 82913-004
ndc11 (package): 82913000401
spl id: 47433424-5a70-96b0-e063-6394a90a269f
spl set id: 6bcd35f5-18ea-4fc8-84cd-06db73f38a1e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.