Hand Sanitizer

Manufacturer: ElEEO Brands LLC | OraLabs
Effective date: 2024-03-02
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:10:30

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

For handwashing to decrease bacteria on the skin that may cause disease. Recommended for repeat use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (63.00%) v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

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.

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin that may cause disease. Recommended for repeat use.

Warnings

WARNINGS SECTION

For external use only: Hands. Flammable. Keep away from flame. When using this product. Keep out of eyes. In case of contact with eye, flush thoroughly with water. Avoid contact with broken skin. Stop use and ask a doctor if skin irritation develops.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Dimethicone, Disodium EDTA, Fragrance, Helianthus Annuus (Sunflower) Seed Oil, Polysorbate 20, Propanediol, Sorbitan Oleate, Water.

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Products#

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

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

Hand Sanitizer
Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79747-008	79747-008-01

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
Name	UNII	Kind
WATER	059QF0KO0R	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
12b0bb8b-e8f5-c885-e063-6294a90a7d6e			813275da-0edb-4bba-b0a4-bca9822b39bf	2024-03-02	Warnings	Exact identifier spl id: 12b0bb8b-e8f5-c885-e063-6294a90a7d6e spl set id: 813275da-0edb-4bba-b0a4-bca9822b39bf

Reported adverse events (FAERS/openFDA)#

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