FDA.reportPublic FDA data

Ollie Toothpaste, Fresh Mint

Manufacturer
Brio Product Group LLC.
Effective date
2026-08-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-08 02:01:43

Label at a glance#

ProductOllie Fresh Mint
Active ingredientSODIUM FLUORIDE, POTASSIUM NITRATE
Label structure6 sections

Indications and uses

Helps protect against cavities

Dosage and administration

• Adults and children 2 years and older: brush teeth thoroughly after meals or at least twice a day or us as directed by a dentist • Do not swallow • To minimize swallowing use a pea-sized amount in children under 6. •  Supervise children’s brushing until good habits • Children under 2 years ask a dentist.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.24%
Potassium Nitrate 5%

Purpose

OTC - PURPOSE SECTION

Anti-cavity
Sensitivity

Uses

INDICATIONS & USAGE SECTION

  • Helps protect against cavities

Warnings

WARNINGS SECTION

Keep out of reach of children under 6 years of age.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for brushing is accidentally swallowed, get medical help or contact a poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Adults and children 2 years and older: brush teeth thoroughly after meals or at least twice a day or us as directed by a dentist
• Do not swallow • To minimize swallowing use a pea-sized amount in children under 6. •  Supervise children’s brushing until good habits • Children under 2 years ask a dentist.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sorbitol, Hydrated Silica, Water (Aqua), Glycerin, Xylitol, Cocos Nucifera (Coconut) Oil, Sodium Lauryl Sulfate, Flavor, Menthol, Aloe Barbadensis Leaf Extract, Xanthan Gum, Hydroxyapatite, Calcium Carbonate, Titanium Dioxide, Cocamidopropyl Betaine, Stevia Rebaudiana Leaf/Stem Extract

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87493-00087493-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM FLUORIDE8ZYQ1474W7ACTIM
POTASSIUM NITRATERU45X2JN0ZACTIB
SORBITOL506T60A25RIACT
HYDRATED SILICAY6O7T4G8P9IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
XYLITOLVCQ006KQ1EIACT
COCONUT OILQ9L0O73W7LIACT
SODIUM LAURYL SULFATE368GB5141JIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
ALOE VERA LEAFZY81Z83H0XIACT
XANTHAN GUMTTV12P4NEEIACT
HYDROXYAPATITE91D9GV0Z28IACT
CALCIUM CARBONATEH0G9379FGKIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
STEVIA REBAUDIANA LEAF6TC6NN0876IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-06-02daily-update2026-06-04 05:10:11

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
Ollie Fresh MintSODIUM FLUORIDE, POTASSIUM NITRATEBrio Product Group LLC.ebeec44f-3c22-43f2-9256-6ece6025c1052026-08-06WarningsExact identifier
ndc (package): 87493-000-01
ndc (product): 87493-000
ndc11 (package): 87493000001
spl id: 58657597-e70f-1324-e063-6394a90a8ac9
spl set id: ebeec44f-3c22-43f2-9256-6ece6025c105

Reported adverse events (FAERS/openFDA)#

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