MAXIMUM SECURITY- sodium fluoride gel, dentifrice

Maximum Security by

Drug Labeling and Warnings

Maximum Security by is a Otc medication manufactured, distributed, or labeled by Bob Barker Company Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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, Flavor, Sodium Hydroxide, Sodium Saccharin, Disodium EDTA, Sodium Benzoate

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 17 g Tube Label

MAXIMUM®
SECURITY

ANTICAVITY
GEL TOOTHPASTE

Sodium Fluoride 0.22%

Fresh Mint Flavor

NET WT 0.6 OZ (17 g)

INGREDIENTS AND APPEARANCE

MAXIMUM SECURITY 
sodium fluoride gel, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53247-132
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium Fluoride (UNII: 8ZYQ1474W7) (Fluoride Ion - UNII:Q80VPU408O)	Sodium Fluoride	2.2 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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)
EDETATE DISODIUM (UNII: 7FLD91C86K)
Sodium Benzoate (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53247-132-01	4.3 g in 1 PACKET; Type 0: Not a Combination Product	01/01/2008
2	NDC: 53247-132-02	17 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2008
3	NDC: 53247-132-03	24 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2008
4	NDC: 53247-132-04	43 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2008
5	NDC: 53247-132-05	130 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2008

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M021	01/01/2008

Labeler - Bob Barker Company Inc. (058525536)