FDA.reportPublic FDA data

ALOE VERA LEAF HAND SANITIZER

Manufacturer
UI Global Brands LLC
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:10:01

Label at a glance#

ProductALOE VERA LEAF HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

To decrease bacteria on the skin and clean hands.  Recommended for repeated use.

Dosage and administration

Apply to hands until thoroughly wet.  Rub vigorously until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin and clean hands.  Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Keep out of reach of children. Do not get into eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If contact occurs, rinse thoroughly with water.

Discontinue use

OTC - STOP USE SECTION

if irritation occurs or redness develops.  If irritation persists for more than 72 hours, consult a doctor.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to hands until thoroughly wet.  Rub vigorously until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Extract, Fragrance (Parfum), Triethanolamine, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate (Vitamin A)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:240ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box2Box2

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
74856-02474856-024-00, 74856-024-01, 74856-024-02

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
WATER059QF0KO0RIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
ALOE VERA LEAFZY81Z83H0XIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
VITAMIN A81G40H8B0TIACT
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
f0479c88-6a08-dcb9-e053-2a95a90a04e8de5274fd-e7b3-4c25-b6c5-f9b369dfd5bc2022-12-20WarningsExact identifier
spl set id: de5274fd-e7b3-4c25-b6c5-f9b369dfd5bc

Reported adverse events (FAERS/openFDA)#

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