L+W Hand Sanitizing Liquid Spray

Manufacturer: Zhejiang Yasili Cosmetics Co., Ltd.
Effective date: 2020-05-20
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:15:43

Label at a glance#

ProductLuxe and Willow Hand Sanitizing Liquid

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

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

Luxe and Willow Hand Sanitizing Liquid
alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74168-002	74168-002-00, 74168-002-01, 74168-002-02, 74168-002-03, 74168-002-04, 74168-002-05, 74168-002-06, 74168-002-07, 74168-002-08, 74168-002-09, 74168-002-10, 74168-002-11, 74168-002-12, 74168-002-13, 74168-002-14, 74168-002-15, 74168-002-16, 74168-002-17, 74168-002-18, 74168-002-19, 74168-002-20, 74168-002-21, 74168-002-22, 74168-002-23, 74168-002-24, 74168-002-25, 74168-002-26, 74168-002-27, 74168-002-28, 74168-002-29, 74168-002-30, 74168-002-31, 74168-002-32, 74168-002-33, 74168-002-34, 74168-002-35, 74168-002-36, 74168-002-37, 74168-002-38, 74168-002-39, 74168-002-40, 74168-002-41, 74168-002-42, 74168-002-43, 74168-002-44, 74168-002-45, 74168-002-46

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
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT

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
d9b6f054-33e8-5b60-e053-2995a90a3a76			a5257e6a-5310-597f-e053-2995a90aed1a	2022-03-08	Warnings	Exact identifier spl set id: a5257e6a-5310-597f-e053-2995a90aed1a

Reported adverse events (FAERS/openFDA)#

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