SALARIUM ANDES SALT PremiumToothpaste

Manufacturer
Aekyung Industrial Co., Ltd.
Effective date
2021-04-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:46:11

Label at a glance#

ProductSALARIUM ANDES SALT PremiumToothpaste
Active ingredientSODIUM FLUORIDE
Label structure7 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium fluoride 0.22%

Use

INDICATIONS & USAGE SECTION

Aids in the prevention of dental decay.

Warnings

WARNINGS SECTION

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

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 right away

Directions

DOSAGE & ADMINISTRATION SECTION

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

Purpose

OTC - PURPOSE SECTION

Anticavity

Inactive ingredients

INACTIVE INGREDIENT SECTION

Liquid Sorbitol, Dental-Type Silica, Water, Sodium Lauryl Sulfate, Flavor, Sodium Chloride, PEG 1500, Carboxymethyl Cellulose Sodium, Saccharin Sodium Hydrate, Xanthan Gum, Pyridoxin Hydrochloride (Vitamin B6), Mineral Salts, Edetate Disodium, Titanium Dioxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

67225-1101-267225-1101-2

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67225-110167225-1101-1, 67225-1101-2

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
dedb297c-f32d-2c75-e053-2a95a90a8479c072d76d-8c12-27e3-e053-2a95a90a01992022-05-12WarningsExact identifier
spl set id: c072d76d-8c12-27e3-e053-2a95a90a0199

Reported adverse events (FAERS/openFDA)#

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