MAXIMUM SECURITY ANTICAVITY GEL FRESH MINT FLAVOR- sodium fluoride paste

Maximum Security Anticavity Gel fresh mint flavor by

Drug Labeling and Warnings

Maximum Security Anticavity Gel fresh mint flavor by is a Otc medication manufactured, distributed, or labeled by SPARROW LIFE CARE PRIVATE LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Sodium Fluoride 0.22 % ( 0.1 % W/V Fluoride Ion)

Purpose

Anticavity Toothpaste

Uses

Help 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

KEEP OUT OF REACH OF CHILDREN

Directions

• Adults & children 6 years of age & older: Brush teeth thoroughly, Preferably after each meal of at least twice a day, or as directed by a dentist or doctor
• Children 2 to 6 years: Use only 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

Product label

INGREDIENTS AND APPEARANCE

MAXIMUM SECURITY ANTICAVITY GEL FRESH MINT FLAVOR 
sodium fluoride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85891-008
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM SACCHARIN (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE DISODIUM (UNII: 7FLD91C86K)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85891-008-01	1000 in 1 BOX	08/01/2025
1		4.25 g in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 85891-008-02	144 in 1 CARTON	08/01/2025
2		43 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	08/01/2025

Labeler - SPARROW LIFE CARE PRIVATE LIMITED (767599018)