FDA.reportPublic FDA data

K-Hand Sanitizer

Manufacturer
UI COSMETICS CO., LTD
Effective date
2020-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:06

Label at a glance#

ProductK-Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

To help reduce bacteria on the skin

Dosage and administration

Apply a small amount in your palm and rub hands together briskly until dry. Supervise children under 6 years in the use of product.

Storage and handling

Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 75%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USES

DOSAGE & ADMINISTRATION SECTION

To help reduce bacteria on the skin

WARNINGS

WARNINGS SECTION

For external use only.

Flammable, keep away from heat or flames.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

keep away from eyes. In case of eye contact, rinse eyes with water.

STOP USE AND ASK DOCTOR IF

OTC - ASK DOCTOR SECTION

irritation and redness develop and persist.

DIRECTIONS

INDICATIONS & USAGE SECTION

Apply a small amount in your palm and rub hands together briskly until dry.

Supervise children under 6 years in the use of product.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Glycerin, Aloe Vera, Tocopheryl Acetate

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60ml NDC: 75615-0030-0 Label60ml NDC: 75615-0030-0 Label

100ml NDC: 75615-0030-1 Label100ml NDC: 75615-0030-1 Label

250ml NDC: 75615-0030-2 Label250ml NDC: 75615-0030-2 Label

300ml NDC: 75615-0030-3 Label300ml NDC: 75615-0030-3 Label

500ml NDC: 75615-0030-4 Label500ml NDC: 75615-0030-4 Label

1000ml NDC: 75615-0030-5 Label1000ml NDC: 75615-0030-5 Label

3785ml NDC: 75615-0030-6 Label3785ml NDC: 75615-0030-6 Label

5000ml NDC: 75615-0030-7 Label5000ml NDC: 75615-0030-7 Label

10000ml NDC: 75615-0030-8 Label10000ml NDC: 75615-0030-8 Label

18750ml NDC: 75615-0030-9 Label18750ml NDC: 75615-0030-9 Label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75615-003075615-0030-0, 75615-0030-1, 75615-0030-2, 75615-0030-3, 75615-0030-4, 75615-0030-5, 75615-0030-6, 75615-0030-7, 75615-0030-8, 75615-0030-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
b7a92b17-ae1f-7d29-e053-2995a90a402cab7c711f-8f28-be06-e053-2995a90a64842020-12-30WarningsExact identifier
spl set id: ab7c711f-8f28-be06-e053-2995a90a6484

Reported adverse events (FAERS/openFDA)#

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