dentalux coconut minerals

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 21:33:34

Label at a glance#

Productdentalux coconut minerals
Active ingredientSODIUM FLUORIDE
Label structure9 sections

Indications and uses

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

Label contents#

Full prescribing information#

active ingredient

OTC - ACTIVE INGREDIENT SECTION

sodium fluoride 0.239% (0.15% w/v fluoride ion)

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Purpose

OTC - PURPOSE SECTION

Anticavity

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Uses

INDICATIONS & USAGE SECTION

Aids in the prevention of dental cavities.

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Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 years of age.

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Warnings

WARNINGS 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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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.
■ do not swallow.
■ to minimize swallowing
use a pea-sized amount in
childred under 6.
■ teach children under 6
years of age good brushing
and rinsing habits until
capable of using without
supervision.
■ children under 2 years of age:
consult a dentist or doctor.

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Inactive ingredients

INACTIVE INGREDIENT SECTION

sorbitol, water, hydrated silica,
sodium bicarbonate, propylene glycol,
tetrapotassium pyrophosphate, sodium
C14-16 olefin sulfonate, disodium
pyrophosphate, titanium dioxide, flavor,
cellulose gum, sodium saccharin, zinc
chloride, menthol.

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Questions

OTC - QUESTIONS SECTION

1-844-656-5151

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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.

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71141-17571141-175-32, 71141-175-00

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
f81f60fc-6cd1-3b40-e053-6394a90a5cd1c60f7935-850c-bda8-e053-2995a90a9e362023-03-30WarningsExact identifier
spl id: f81f60fc-6cd1-3b40-e053-6394a90a5cd1
spl set id: c60f7935-850c-bda8-e053-2995a90a9e36

Reported adverse events (FAERS/openFDA)#

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