MAXIMUM SECURITY- sodium fluoride gel, dentifrice 
Bob Barker Company Inc.

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Maximum® Security

Drug Facts

Active ingredient

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

Purpose

Anticavity toothpaste

Use

Helps protect against cavities.

Warnings

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

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

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

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

PRINCIPAL DISPLAY PANEL - 43 g Tube Label

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
MAXIMUM SECURITY 
sodium fluoride gel, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53247-130
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Fluoride (UNII: 8ZYQ1474W7) (Fluoride Ion - UNII:Q80VPU408O) Sodium Fluoride2.2 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Sorbitol (UNII: 506T60A25R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
Sodium Lauryl Sulfate (UNII: 368GB5141J)  
Sodium Hydroxide (UNII: 55X04QC32I)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
Sodium Benzoate (UNII: OJ245FE5EU)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53247-130-014.3 g in 1 PACKET; Type 0: Not a Combination Product01/01/2008
2NDC:53247-130-0217 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
3NDC:53247-130-0324 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
4NDC:53247-130-0443 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
5NDC:53247-130-05130 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM02101/01/2008
Labeler - Bob Barker Company Inc. (058525536)

Revised: 2/2024
Document Id: 3d24a0e7-3e0d-495b-a3ba-1ca883da5ae5
Set id: e29f30ec-72ea-4944-a2c2-b1696d31b639
Version: 2
Effective Time: 20240227
 
Bob Barker Company Inc.