Dr. Zenni Tooth for Sensitive Tooth

Manufacturer
Zeniton Co.,Ltd. | DONG IL PHARMS CO., LTD.
Effective date
2019-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:25:48

Label at a glance#

ProductDr. Zenni Tooth for Sensitive Tooth
Active ingredient.ALPHA.-TOCOPHEROL ACETATE, SILICON DIOXIDE, TRIBASIC CALCIUM PHOSPHATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Dental Type Silica, Tricalcium Phosphate, 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

A proper amount of toothpaste is put on the toothbrush and the tooth is cleaned by brushing.

WARNINGS SECTION

Storage method

1. Keep it at room temperature in a classified container.

2. Cover and store at room temperature.

3. Store in a not moisture and cool place.

4. Air may come out during use of this product, but there is no problem with its weight.

Usage Precautions

1. Be careful not to swallow. Rinse mouth thoroughly after use

2. If the use of toothpaste causes abnormalities such as gums or mouth injury, discontinue use and consult a doctor or dentist.

3. For children under 6 years of age, use a small amount of toothpaste as small as pea per use, and use under the guidance of a guardian to avoid sucking or swallowing.

4. If a child under 6 years old swallows large amount, consult with a doctor or dentist immediately.

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

INACTIVE INGREDIENT SECTION

D-Sorbitol Solution
Concentrated Glycerin
Xanthangum
Chamomile Extract
Sage Extract
Aloe Extract
Eucalyptus Extract
Grapefruit Seed Extract
Sodium Chloride
Xylitol
Enzymatically Modified Stevia
L-Menthol
Red Wine Flavor
Peppermint Oil
Mastic Oil
Hydroxyapatite
Sodium Cocoyl Glutamate
Aqua

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73029-000773029-0007-1

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
651b2d9d-330f-4f08-aef2-921e8197bf3c86b08d6a-51ad-3129-e053-2a91aa0a50372021-12-17WarningsExact identifier
spl set id: 86b08d6a-51ad-3129-e053-2a91aa0a5037

Reported adverse events (FAERS/openFDA)#

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