Maximum Security Anticavity Gel fresh mint flavor

Manufacturer
SPARROW LIFE CARE PRIVATE LIMITED
Effective date
2025-08-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:11:37

Label at a glance#

ProductMaximum Security Anticavity Gel fresh mint flavor
Active ingredientSODIUM FLUORIDE
Label structure7 sections

Indications and uses

• Help Protect against cavities

Dosage and administration

 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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

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

Purpose

OTC - PURPOSE SECTION

Anticavity Toothpaste

Uses

INDICATIONS & USAGE SECTION

• Help Protect against cavities

Warnings

WARNINGS 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 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

INACTIVE INGREDIENT SECTION

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

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
245598sodium fluoride 0.22 % ToothpastePSN1
245598sodium fluoride 0.0022 MG/MG ToothpasteSCD1
245598sodium fluoride 0.22 % (fluoride 0.1 % ) ToothpasteSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85891-008-01Maximum Security Anticavity Gel fresh mint flavor4.25 g in 1 PACKAGEPASTE4.251
85891-008-01Maximum Security Anticavity Gel fresh mint flavor1000 in 1 BOXPASTE10001
85891-008-02Maximum Security Anticavity Gel fresh mint flavor43 g in 1 TUBEPASTE431
85891-008-02Maximum Security Anticavity Gel fresh mint flavor144 in 1 CARTONPASTE1441

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
85891-00885891-008-01, 85891-008-02

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
3d2ff13b-c493-855d-e063-6394a90a2b0d268a5cc3-b688-490d-b64c-9cb51fe7560d2025-08-25WarningsExact identifier
spl id: 3d2ff13b-c493-855d-e063-6394a90a2b0d
spl set id: 268a5cc3-b688-490d-b64c-9cb51fe7560d

Reported adverse events (FAERS/openFDA)#

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