FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
GREENERWAYS LLC
Effective date
2020-12-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:58:22

Label at a glance#

ProductHAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

FOR HAND WASHING TO REDUCE BACTERIA ON SKIN.

Dosage and administration

PUMP INTO DRY HANDS. LATHER VIGOROUSLY FOR AT LEAST 15 SECONDS. RINSE AND DRY THOROUGHLY.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

FOR HAND WASHING TO REDUCE BACTERIA ON SKIN.

WARNINGS

WARNINGS SECTION

FOR ESTERNAL USE ONLY.

WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS DEVELOP.

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 RIGHT AWAY.

(1-800-222-1222)

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

PUMP INTO DRY HANDS. LATHER VIGOROUSLY FOR AT LEAST 15 SECONDS. RINSE AND DRY THOROUGHLY.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER (AQUA), SODIUM C14-16 OLEFIN SULFONATE, COCAMIDOPROPYL HYDROXYSULTAINE, ALOE BARBADENSIS LEAF JUICE, SODIUM COCOYL ISETHIONATE, SODIUM PCA, PROPYLENE GLYCOL, GLYCERIN, COCAMIDE MIPA, ZINC GLUCONATE, POLYQUATERNIUM-10, PANTHENOL, COPPER GLUCONATE, CITRIC ACID

QUESTIONS?

OTC - QUESTIONS SECTION

1-800-777-1603

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_GW_HandSoap_Mockup_Front_03262001b LBL_GW_HandSoap_Mockup_Front_032620

01b LBL_GW_HandSoap_Mockup_Back_03262001b LBL_GW_HandSoap_Mockup_Back_032620

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74487-10274487-102-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
SODIUM C14 OLEFIN SULFONATEN816E2SOKIIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM COCOYL ISETHIONATE518XTE8493IACT
SODIUM PYRROLIDONE CARBOXYLATE469OTG57A2IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
COCO MONOISOPROPANOLAMIDE21X4Y0VTB1IACT
ZINC GLUCONATEU6WSN5SQ1ZIACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
PANTHENOLWV9CM0O67ZIACT
COPPER GLUCONATERV823G6G67IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT

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
cee32383-8f5c-b483-e053-2a95a90a23f615bfe959-25ea-435e-8c92-b09fb0407d4b2021-10-21WarningsExact identifier
spl set id: 15bfe959-25ea-435e-8c92-b09fb0407d4b

Reported adverse events (FAERS/openFDA)#

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