FDA.reportPublic FDA data

Hand Kleen Foaming Antibacterial Hand Cleanser

Manufacturer
Auto-Chlor System
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:07:14

Label at a glance#

ProductHand Kleen Foaming Antibacterial Hand Cleanser
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.26% w/w

OTC - PURPOSE SECTION

Antiseptic handwash

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

WARNINGS SECTION

For external use only.

When using this product, do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

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

INSTRUCTIONS FOR USE SECTION

Wet hands and forearms.

Apply 5mL or palmful to hand and forearms.

Scrub thoroughly for at least 15 seconds.

Rinse completely and dry.

INACTIVE INGREDIENT SECTION

Water, laurmine oxide, _cetyl trimethyl ammonium chloride, _lauryl lactyl lactate, polyoxyethelene (7) glyceryl monococoate, DMDM hydantoin, Disodium ethylenediamine tetraacetate, frangrance, 2-propen-1 aminium, N,N-dimethyl-N-2-propenyl-, chloride polymer with 2-propenamide

DOSAGE & ADMINISTRATION SECTION

Directions

Wet hands and forearms.

Apply 5 mL or palmful to hand and forearms.

Scrub thoroughly for at least 15 seconds.

Rinse completely and dry.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

ACL30241 HK Foaming Antibacterial Hand Cleanser 1000ml Label 355.21

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ACL30241 HK Foaming Antibacterial Hand Cleanser 1000ml Label 355.21.jpgACL30241 HK Foaming Antibacterial Hand Cleanser 1000ml Label 355.21.jpgACL30241 HK Foaming Antibacterial Hand Cleanser 1000ml Label 355.21.jpg

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
68604-24168604-241-01, 68604-241-02

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
DMDM HYDANTOINBYR0546TOWIACT
DISODIUM ETHYLENEDIAMINEDIACETATEEQL53S5L0FIACT
LAURYL LACTYL LACTATE, DL-M96FF85L6ZIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
LAURAMINE OXIDE4F6FC4MI8WIACT

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
f10d1b37-a870-7739-e053-2a95a90a31ded4c4a324-0a9a-b602-e053-2a95a90afe692022-12-30WarningsExact identifier
spl set id: d4c4a324-0a9a-b602-e053-2a95a90afe69

Reported adverse events (FAERS/openFDA)#

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