Glister Multi-Action

Manufacturer
Access Business Group LLC
Effective date
2023-10-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:57:23

Label at a glance#

ProductGlister Multi-Action
Active ingredientSODIUM FLUORIDE
Label structure7 sections

Dosage and administration

• Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. • Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. • Children under 2 years of age: Consult a dentist or doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.21%

Purpose

OTC - PURPOSE SECTION

Anticavity

Use

INDICATIONS & USAGE SECTION

Aids in the prevention of dental cavities.

Warnings

WARNINGS SECTION

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately. under 6 years of age.

Directions

DOSAGE & ADMINISTRATION SECTION

• Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.

• Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing).

Supervise children as necessary until capable of using without supervision.

• Children under 2 years of age: Consult a dentist or doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Sorbitol, Hydrated Silica, Glycerin, Propylene Glycol, Sodium Lauryl Sulfate, Xylitol, Cellulose Gum, PEG-8, Flavor, Titanium Dioxide, Sodium Benzoate, Xanthan Gum, Sodium Saccharin, Blue No. 1

Package Labeling:50g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label50gLabel50g

Package Labeling:200g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label200gLabel200g

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1099038sodium fluoride 0.21 % ToothpastePSN2
1099038sodium fluoride 0.0021 MG/MG ToothpasteSCD2
1099038sodium fluoride 0.21 % ToothpasteSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10056-415-00Glister Multi-Action50 g in 1 TUBEPASTE, DENTIFRICE502
10056-415-00Glister Multi-Action1 in 1 CARTONPASTE, DENTIFRICE12
10056-415-01Glister Multi-Action1 in 1 CARTONPASTE, DENTIFRICE12
10056-415-01Glister Multi-Action200 g in 1 TUBEPASTE, DENTIFRICE2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10056-415GLISTER MULTI-ACTION (SODIUM FLUORIDE) PASTE, DENTIFRICE [ACCESS BUSINESS GROUP LLC]2Current NDC, 4 package rows20231023_e3f2c049-a0f5-4649-a4aa-11bdb252f951.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10056-41510056-415-00, 10056-415-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 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
Glister Multi-ActionSODIUM FLUORIDEAccess Business Group LLCe3f2c049-a0f5-4649-a4aa-11bdb252f9512023-10-23WarningsExact identifier
ndc (package): 10056-415-00
ndc (package): 10056-415-01
ndc (product): 10056-415
ndc11 (package): 10056041501
ndc11 (package): 10056041500
spl id: 085bbc1a-0302-ea11-e063-6394a90a3391
spl set id: e3f2c049-a0f5-4649-a4aa-11bdb252f951

Reported adverse events (FAERS/openFDA)#

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