Ecological Alcohol Free Hand Sanitizer

Manufacturer
HUNTER AMENITIES INTL. LTD
Effective date
2020-10-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:11:47

Label at a glance#

ProductEcological Alcohol Free Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Indications and uses

• Antiseptic (skin) cleanser • Medicated (skin) cleanser • Antibacterial (skin) cleanser • Kills harmful bacteria/germs • Effective in destroying (harmful) bacteria to provide antiseptic cleansing • For personal hand hygiene to help prevent the spread of bacteria

Dosage and administration

Adults and children over 2 years: • For occasional and personal domestic use. • Supervise children when they use this product. • Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Label contents#

Full prescribing information#

Active ingredient (v/v)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13 %

Purpose

OTC - PURPOSE SECTION

Antiseptic skin cleanser

Uses

INDICATIONS & USAGE SECTION

• Antiseptic (skin) cleanser • Medicated (skin) cleanser • Antibacterial (skin) cleanser
• Kills harmful bacteria/germs • Effective in destroying (harmful) bacteria to provide antiseptic cleansing • For personal hand hygiene to help prevent the spread of bacteria

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask/ consult a doctor/

OTC - STOP USE SECTION

physician/ health care practitioner/ health care provider/ health care professional if irritation develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a poison control centre or get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years: • For occasional and personal domestic use. • Supervise children when they use this product. • Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, Propylene Glycol, Glycerin, Hydroxyethylcellulose, Phenoxyethanol, Ethylhexylglycerin, Aloe Barbadensis Leaf Juice

Questions?

OTC - QUESTIONS SECTION

1-800-668-1483

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabel2Label2

Package Labeling:30 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:50 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:120 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

Package Labeling:3700 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4Bottle4

Package Labeling:300 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle5Bottle5

Package Labeling:650 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle6Bottle6

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65910-00565910-005-01, 65910-005-02, 65910-005-03, 65910-005-04, 65910-005-05, 65910-005-06, 65910-005-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
cdb28cb7-4931-04b6-e053-2995a90a629111f4ccfa-e312-49cc-8541-9d15be09c1412021-10-06WarningsExact identifier
spl set id: 11f4ccfa-e312-49cc-8541-9d15be09c141

Reported adverse events (FAERS/openFDA)#

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