FDA.reportPublic FDA data

Aloe Vera Hand Sanitizer

Manufacturer
Ni Hau Industrial Co., Ltd.
Effective date
2022-01-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:18:57

Label at a glance#

ProductAloe Vera Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Squeeze a sufficient amount on hands. Rub together until dry.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away for fire and flames.

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of eye contact, flush with water. Do not inhale or ingest. Keep out of reach of children.

OTC - STOP USE SECTION

Stop Use and ask a doctor if skin irritation develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Squeeze a sufficient amount on hands. Rub together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Water, Propanediol, Polyacrylic Acid (Carbomer), Aminomethyl Propanol, Melaleuca alternifolia (Tea Tree) Oil, Methylparaben, Sodium Benzoate, Citric Acid, Cyclohexane, Potassium Sorbate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front and Back LabelsFront and Back Labels45 mL NDC: 77189-007-45

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77189-00777189-007-45

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID ACETATEDSO12WL7AUIACT
POLYACRYLIC ACID (250000 MW)9G2MAD7J6WIACT
SODIUM BENZOATEOJ245FE5EUIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
TEA TREE OILVIF565UC2GIACT
METHYLPARABENA2I8C7HI9TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CYCLOHEXANE48K5MKG32SIACT
PROPANEDIOL5965N8W85TIACT

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
f1266117-071c-8d11-e053-2995a90ac744a7b23b54-a3a7-9753-e053-2995a90a6e7f2022-12-31WarningsExact identifier
spl set id: a7b23b54-a3a7-9753-e053-2995a90a6e7f

Reported adverse events (FAERS/openFDA)#

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