Luxe & Willow Hand Sanitizer Spray

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78713-00178713-001-08

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
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
f049ba4a-af78-c769-e053-2a95a90aec9caaa7c69c-1f2d-7ab2-e053-2995a90a80d42022-12-20WarningsExact identifier
spl id: f049ba4a-af78-c769-e053-2a95a90aec9c
spl set id: aaa7c69c-1f2d-7ab2-e053-2995a90a80d4

Reported adverse events (FAERS/openFDA)#

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