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Maximum Security by Bob Barker Company Inc.

Medically reviewed on Dec 12, 2017

Dosage form: gel, dentifrice
Ingredients: Sodium Fluoride 2.2mg in 1g
Labeler: Bob Barker Company Inc.
NDC Code: 53247-109

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Maximum Security®

DRUG FACTS

ACTIVE INGREDIENT

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

PURPOSE

Anticavity.

USE

Helps protect against 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 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 physician.
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

Purified Water, Sorbitol, Carbopol, Sodium Lauryl Sulfate, Flavor, Polyethylene Glycol 1500, Sodium Saccharin, Precipitated Silica, Sodium Carboxymethyl Cellulose, Methylparaben, Propylparaben.

PRINCIPAL DISPLAY PANEL - 78 g Tube Label

MAXIMUM
SECURITY
®

GEL TOOTHPASTE

NET WT. 2.75 OZ. (78 g)

MAXIMUM SECURITY 
sodium fluoride gel, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53247-109
Route of AdministrationDENTALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Fluoride (Fluoride Ion) Fluoride Ion2.2 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Water 
Sorbitol 
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) 
Sodium Lauryl Sulfate 
Polyethylene Glycol 1500 
Saccharin Sodium 
Silicon Dioxide 
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 
Methylparaben 
Propylparaben 
Packaging
#Item CodePackage Description
1NDC:53247-109-014.3 g in 1 PACKET
2NDC:53247-109-0217 g in 1 TUBE
3NDC:53247-109-0324 g in 1 TUBE
4NDC:53247-109-0443 g in 1 TUBE
5NDC:53247-109-0578 g in 1 TUBE
6NDC:53247-109-06130 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35501/01/2008
Labeler - Bob Barker Company Inc. (058525536)

 
Bob Barker Company Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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