K-MOM ZERO-DUST RAINBOW HAND SANITIZER

Manufacturer: MOTHER-K CO.,LTD | DONG IL PHARMS CO., LTD.
Effective date: 2020-04-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:37:55

Label at a glance#

ProductK-MOM ZERO-DUST RAINBOW HAND SANITIZER

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

For the external use only

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

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

DOSAGE & ADMINISTRATION SECTION

No dilution is required. Use it by immersing or spraying it where you want. No additional cleaning process is required after use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

K-MOM ZERO-DUST RAINBOW HAND SANITIZER
Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73429-0004	73429-0004-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d533f125-4ee9-5adf-e053-2995a90aec69			a24a8890-934e-569f-e053-2995a90abd1b	2022-01-09	Warnings	Exact identifier spl set id: a24a8890-934e-569f-e053-2995a90abd1b

Reported adverse events (FAERS/openFDA)#

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