CleanAFNaturalAnticavityToothpaste

Manufacturer
CLEANAF GLOBAL LIMITED LIABILITY COMPANY
Effective date
2017-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:51:59

Label at a glance#

ProductCleanAFNaturalAnticavityToothpaste
Active ingredientSODIUM FLUORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ToothpasteToothpaste

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.22% (0.10% w/v fluoride ion)

INACTIVE INGREDIENT SECTION

Hydrated Silica, sodium benzoate, sodium lauryl sulfate, water, flavor, sorbitol, CMC, xantham gum, sodium phytate, sodium saccharin, titanium dioxide, glycerin​

OTC - PURPOSE SECTION

Anticavity

DOSAGE & ADMINISTRATION SECTION

WARNINGS SECTION

Do not swallow

INDICATIONS & USAGE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71603-1700-02020-01-31C16284748780-19d75b9d1-0fab-f424-e053-dadaa90a57ceCleanAF Toothpaste

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71603-1700-0CleanAFNaturalAnticavityToothpaste142 g in 1 TUBEPASTE1421

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71603-1700CLEANAFNATURALANTICAVITYTOOTHPASTE (SODIUM FLUROIDE PASTE, DENTRIFICE) PASTE [CLEANAF GLOBAL LIMITED LIABILITY COMPANY]1Legacy NDC, 1 package rows20170719_544b9ca2-f66e-526a-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71603-170071603-1700-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
544b9ca2-f66f-526a-e054-00144ff88e88544b9ca2-f66e-526a-e054-00144ff88e882017-07-14WarningsExact identifier
spl id: 544b9ca2-f66f-526a-e054-00144ff88e88
spl set id: 544b9ca2-f66e-526a-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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