KUNDAL Sensitive Dental Care Tooth (Apple Chamomile Mint)

Manufacturer
THESKINFACTORY Co., Ltd. | DONG IL PHARMS CO., LTD.
Effective date
2020-09-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:15:31

Label at a glance#

ProductKUNDAL Sensitive Dental Care Tooth (Apple Chamomile Mint)
Active ingredientTRIBASIC CALCIUM PHOSPHATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Tricalcium Phosphate

INACTIVE INGREDIENT SECTION

Sorbitol
Water
Sodium Cocoyl Glutamate
Cellulose Gum
PEG-32
Apple chamomile mint flavor
Menthol
Sodium Benzoate
Xylitol
Stevioside
Camellia Sinensis Leaf Extract
Aloe Barbadensis Leaf Extract
Chamomilla Recutita (Matricaria) Flower Extract
Salvia Officinalis (Sage) Leaf Extract
Eucalyptus Globulus Leaf Extract

OTC - PURPOSE SECTION

for dental care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE 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 doctor.

Children 2 to 6 years of age: Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision.

Children under 2 years of age: Consult a dentist or doctor.

WARNINGS SECTION

Do not swallow.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128X002ML5VFPlabel-camop.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74773-0040-12024-12-12C16284748780-1e4f33bdf-a376-d8a0-e053-dadaa90a6e4eDrug Facts
74773-0040-12022-07-29C16284748780-1e4f33bdf-a376-d8a0-e053-dadaa90a6e4eDrug Facts

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74773-004074773-0040-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
290f3dd9-2342-8568-e063-6294a90a672faf3cb338-1bff-5b78-e053-2995a90a13102024-12-12WarningsExact identifier
spl set id: af3cb338-1bff-5b78-e053-2995a90a1310

Reported adverse events (FAERS/openFDA)#

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