Luxe & Willow Hand Sanitizer Gel

Manufacturer: MiWorld Accessories LLC
Effective date: 2022-12-20
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:43:51

Label at a glance#

ProductLuxe and Willow Hand Sanitizer

Active ingredientALCOHOL

Label structure6 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.

Do not use

OTC - DO NOT USE SECTION

in or near eyes. In case of contact, rinse thoroughly with water

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop and persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 Alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

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

Luxe and Willow Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
EDETOL
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78713-002	78713-002-08

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
EDETOL	Q4R969U9FR	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALCOHOL	3K9958V90M	ACTIB

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
f049d9f5-9d08-4781-e053-2a95a90aefe5			aaa72cb4-2742-3418-e053-2995a90aca20	2022-12-20	Warnings	Exact identifier spl id: f049d9f5-9d08-4781-e053-2a95a90aefe5 spl set id: aaa72cb4-2742-3418-e053-2995a90aca20

Reported adverse events (FAERS/openFDA)#

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