FDA.reportPublic FDA data

Luxe and Willow Hand Sanitizer

Manufacturer
Zhejiang Yasili Cosmetics Co., Ltd.
Effective date
2020-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:07

Label at a glance#

ProductLuxe and Willow Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

To decrease bacteria on skin without soap or water Recommended for repeated use

Dosage and administration

Put enough product on palm and rub hands until dry Children under 6 years of age should be supervised while using this product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on skin without soap or water
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only. Only on hands.

Flammable, keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use in or near eyes. In case of contact, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product on palm and rub hands until dry
  • Children under 6 years of age should be supervised while using this product

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, glycerin, acrylates/C10-30 aklykl acrylate crosspolymer, tetrahydroxypropyl ethylenediamine, aloe barbadensis leaf extract, tocopheryl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label 1label 1

label 2label 2

label 3label 3

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74168-00174168-001-00, 74168-001-01, 74168-001-02, 74168-001-03, 74168-001-04, 74168-001-05, 74168-001-06, 74168-001-07, 74168-001-08, 74168-001-09, 74168-001-10, 74168-001-11, 74168-001-12, 74168-001-13, 74168-001-14, 74168-001-15, 74168-001-16, 74168-001-17, 74168-001-18, 74168-001-19, 74168-001-20, 74168-001-21, 74168-001-22, 74168-001-23, 74168-001-24, 74168-001-25, 74168-001-26, 74168-001-27, 74168-001-28, 74168-001-29, 74168-001-30, 74168-001-31, 74168-001-32, 74168-001-33, 74168-001-34, 74168-001-35, 74168-001-36, 74168-001-37, 74168-001-38, 74168-001-39, 74168-001-40, 74168-001-41, 74168-001-42, 74168-001-43, 74168-001-44, 74168-001-45, 74168-001-46

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
ALOE VERA LEAFZY81Z83H0XIACT
EDETOLQ4R969U9FRIACT
ALCOHOL3K9958V90MACTIB
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT

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
d9b6e7e8-3bba-49a1-e053-2a95a90aaf41a524322c-7b2e-11b4-e053-2a95a90a19782022-03-08WarningsExact identifier
spl set id: a524322c-7b2e-11b4-e053-2a95a90a1978

Reported adverse events (FAERS/openFDA)#

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