Dentalux total care

Manufacturer
Lidl US LLC
Effective date
2023-03-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:33:33

Label at a glance#

ProductDentalux total care
Active ingredientSODIUM FLUORIDE
Label structure8 sections

Indications and uses

helps protect against dental cavities tube: box:

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 use as directed by a dentist or doctor - do not swallow - to minimize swallowing use a pea-sized amount in children under 6 years of age - teach children under 6 years of age good brushing and rinsing habits until capable of using without supervision Children under 2 years of age: cosult a d...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Sodium fluoride 0,243% (0,14% w/v fluoride ion)

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Purpose

OTC - PURPOSE SECTION

Anticavity

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Uses

INDICATIONS & USAGE SECTION

helps protect against dental cavities

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Keep out of reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of 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 right away.

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Warnings

WARNINGS SECTION

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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 use as directed by a dentist or doctor

- do not swallow

- to minimize swallowing use a pea-sized amount in children under 6 years of age

- teach children under 6 years of age good brushing and rinsing habits until capable of using without supervision

Children under 2 years of age: cosult a dentist or doctor

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Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sorbitol, hydrated silica, propylene glycol, potassium nitrate, glycerin, sodium C14-16 olefin sulfonate, flavor, xanthan gum, menthol, sodium saccharin, zinc chloride, titanium dioxide

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pdp

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
71141-17071141-170-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
f81f6d80-0772-16a6-e053-6294a90ab148c17f010a-f73d-5191-e053-2a95a90af4682023-03-30WarningsExact identifier
spl id: f81f6d80-0772-16a6-e053-6294a90ab148
spl set id: c17f010a-f73d-5191-e053-2a95a90af468

Reported adverse events (FAERS/openFDA)#

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