K-MOM Kids Tooth

Manufacturer: MOTHER-K CO.,LTD | KMPHARMACEUTICAL Co.,Ltd.
Effective date: 2019-11-26
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:01:41

Label at a glance#

ProductK-MOM Kids Tooth

Active ingredientSILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Silica, Sodium Monofluorosphate

OTC - PURPOSE SECTION

For dental care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

Brush your teeth with a suitable amount of brush

WARNINGS SECTION

Keep out of the 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

INACTIVE INGREDIENT SECTION

Sorbitol, Water, Glycerin, Stevioside, Hydrated Silica, etc.

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73429-0001-1	2022-07-29	C162847	48780-1	e4f33bdf-a40d-d8a0-e053-dadaa90a6e4e	96900a7d-32bc-2612-e053-2995a90a602a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73429-0001-1	K-MOM Kids Tooth	50 g in 1 TUBE	PASTE, DENTIFRICE	50		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73429-0001	K-MOM KIDS TOOTH (SILICA, SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [MOTHER-K CO.,LTD]	3	Legacy NDC, 1 package rows	20191127_96900a7d-32bc-2612-e053-2995a90a602a.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

K-MOM Kids Tooth
Silica, Sodium Monofluorophosphate
SILICON DIOXIDE
XYLITOL
WATER
SODIUM MONOFLUOROPHOSPHATE
FLUORIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73429-0001	73429-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SILICON DIOXIDE	ETJ7Z6XBU4	ACTIB
XYLITOL	VCQ006KQ1E	IACT
WATER	059QF0KO0R	IACT
SODIUM MONOFLUOROPHOSPHATE	C810JCZ56Q	ACTIM

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
984c119b-0ac5-672a-e053-2a95a90af088			96900a7d-32bc-2612-e053-2995a90a602a	2019-11-26	Warnings	Exact identifier spl id: 984c119b-0ac5-672a-e053-2a95a90af088 spl set id: 96900a7d-32bc-2612-e053-2995a90a602a

Reported adverse events (FAERS/openFDA)#

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