Dr.EL TOOTH WHITE TOOTH

Manufacturer
Dr. EL CO., LTD. | DONG IL PHARMS CO.,LTD
Effective date
2019-09-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:09:48

Label at a glance#

ProductDr.EL TOOTH WHITE TOOTH
Active ingredientSILICON DIOXIDE, .ALPHA.-TOCOPHEROL ACETATE, HYDROGEN PEROXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Colloidal Silicon Dioxide
Hydrogen Peroxide Solution 35 %
Tocopherol Acetate

OTC - PURPOSE SECTION

For dental care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE 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 physician

Children 2 to 6 years: Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)

Children under 2 years: Ask a dentist or physician

WARNINGS SECTION

1. Application precautions

1)Do not use anything other than a brushing teeth.

2)If you've eaten too much of this product, Consult a physician or dentist immediately.

2. Cautions for storage

1)Keep out of the reach of children under of age and If used by children, And use itunder the supervision of a guardian.

2)Avoid direct sunlight and keep the lid at room temperature.

INACTIVE INGREDIENT SECTION

D-Sorbitol Solution, Carboxymethylcellulose Sodium, Aloe Extract, Chamomile Extract, Green Tea Extract, Xylitol, Erythritol, Hydroxyapatite, Eucalyptus Extract, Peppermint Oil, Mint Flavor, L-Menthol, Polysorbate 20, Sodium Cocoyl Glutamate, Aqua

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72440-106-012025-01-03C16284748780-1f386c649-b625-0266-e053-dadaa90a7c1a936ca241-2fe2-d094-e053-2a95a90ac307
72440-106-012023-01-30C16284748780-1f386c649-b625-0266-e053-dadaa90a7c1a936ca241-2fe2-d094-e053-2a95a90ac307

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72440-10672440-106-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
2ac83c34-95dd-c615-e063-6394a90afeb9936ca241-2fe2-d094-e053-2a95a90ac3072025-01-03WarningsExact identifier
spl set id: 936ca241-2fe2-d094-e053-2a95a90ac307

Reported adverse events (FAERS/openFDA)#

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