Plak Smacker

Manufacturer
LMZ
Effective date
2021-03-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:05

Label at a glance#

ProductPlak Smacker Mint Blast
Active ingredientSODIUM FLUORIDE
Label structure7 sections

Indications and uses

Aids in the prevention of cavities

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 a physician. Children 2 to 6 years: To minimize swallowing use a pea sized amount. Supervise children's brushing until good habits are established. Children under 2 years: Ask a dentist or a physician.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.243% (equivalent to 0.13% w/v fluoride ion)

Purpose

OTC - PURPOSE SECTION

Anti-cavity

Uses

INDICATIONS & USAGE SECTION

Aids in the prevention of cavities

Warnings

WARNINGS SECTION

If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children 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 a physician.

Children 2 to 6 years: To minimize swallowing use a pea sized amount. Supervise children's brushing until good habits are established.

Children under 2 years: Ask a dentist or a physician.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sorbitol, Silica, Water, PEG-8, Sodium lauryl sulfate, Flavor, Titanium dioxide, Cellulose gum, Trisodium phosphate, Sodium saccharin, Xanthan gum, Benzyl alcohol, Xylitol, CI 42090

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

28 g NDC: 71775-080-01

Mint Blast 28 gMint Blast 28 g

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
891775sodium fluoride 0.243 % ToothpastePSN1
891775sodium fluoride 0.00243 MG/MG ToothpasteSCD1
891775sodium fluoride 0.243 % (fluoride ion 0.13 % ) ToothpasteSY1
891775sodium fluoride 0.243 % (fluoride ion 0.14 % ) ToothpasteSY1
891775sodium fluoride 0.243 % (fluoride ion 0.15 % ) ToothpasteSY1
891775sodium fluoride 0.243 % (fluoride ion 0.16 % ) ToothpasteSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71775-080-012023-01-30C16284748780-1f386c64a-1519-0266-e053-dadaa90a7c1aMint Blast Toothpaste

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71775-080-01Plak SmackerMint Blast28 g in 1 TUBEPASTE281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71775-080PLAK SMACKER MINT BLAST (SODIUM FLUORIDE) PASTE [LMZ]1Legacy NDC, 1 package rows20210320_bdd574e2-7d94-64b9-e053-2995a90a0386.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71775-08071775-080-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
bdd574e2-7d95-64b9-e053-2995a90a0386bdd574e2-7d94-64b9-e053-2995a90a03862021-03-18WarningsExact identifier
spl id: bdd574e2-7d95-64b9-e053-2995a90a0386
spl set id: bdd574e2-7d94-64b9-e053-2995a90a0386

Reported adverse events (FAERS/openFDA)#

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