Maximum Security

Manufacturer
Bob Barker Company Inc.
Effective date
2024-02-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:09:23

Label at a glance#

ProductMaximum Security
Active ingredientSodium Fluoride
Label structure9 sections

Dosage and administration

Adults & Children 6 years of age & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Children 2 to 6 years: Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing). Children under 2 years: Ask a dentist or physician.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride - 0.22% (0.1% w/v fluoride ion)

Purpose

OTC - PURPOSE SECTION

Anticavity toothpaste

Use

INDICATIONS & USAGE SECTION

Helps protect against cavities.

Warnings

WARNINGS SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the 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 Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults & Children 6 years of age & older:Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.
Children 2 to 6 years:Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing).
Children under 2 years:Ask a dentist or physician.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sorbitol, Carbomer, Sodium Lauryl Sulfate, Sodium Hydroxide, Flavor, Sodium Saccharin, Sodium Benzoate, Disodium EDTA, Menthol

SPL UNCLASSIFIED SECTION

Dist. by Bob Barker Co. Inc. Fuquay-Varina, NC 27526

PRINCIPAL DISPLAY PANEL - 43 g Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAXIMUM®
SECURITY

ANTICAVITY
GEL TOOTHPASTE
Sodium Fluoride 0.22%

Fresh Mint Flavor

NET WT 1.5 OZ. (43 g)

Principal Display Panel - 43 g Tube Label
Principal Display Panel - 43 g Tube Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
245598sodium fluoride 0.22 % ToothpastePSN2
245598sodium fluoride 0.0022 MG/MG ToothpasteSCD2
245598sodium fluoride 0.22 % (fluoride 0.1 % ) ToothpasteSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53247-130-01Maximum Security4.3 g in 1 PACKETGEL, DENTIFRICE4.32
53247-130-02Maximum Security17 g in 1 TUBEGEL, DENTIFRICE172
53247-130-03Maximum Security24 g in 1 TUBEGEL, DENTIFRICE242
53247-130-04Maximum Security43 g in 1 TUBEGEL, DENTIFRICE432
53247-130-05Maximum Security130 g in 1 TUBEGEL, DENTIFRICE1302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53247-130MAXIMUM SECURITY (SODIUM FLUORIDE) GEL, DENTIFRICE [BOB BARKER COMPANY INC.]2Current NDC, 5 package rows20240306_e29f30ec-72ea-4944-a2c2-b1696d31b639.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53247-13053247-130-01, 53247-130-02, 53247-130-03, 53247-130-04, 53247-130-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
Maximum SecuritySODIUM FLUORIDEBob Barker Company Inc.e29f30ec-72ea-4944-a2c2-b1696d31b6392024-02-27WarningsExact identifier
ndc (package): 53247-130-05
ndc (package): 53247-130-02
ndc (package): 53247-130-01
ndc (package): 53247-130-04
ndc (package): 53247-130-03
ndc (product): 53247-130
ndc11 (package): 53247013005
ndc11 (package): 53247013001
ndc11 (package): 53247013003
ndc11 (package): 53247013004
ndc11 (package): 53247013002
spl id: 3d24a0e7-3e0d-495b-a3ba-1ca883da5ae5
spl set id: e29f30ec-72ea-4944-a2c2-b1696d31b639

Reported adverse events (FAERS/openFDA)#

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