ATOREN PREMIUM HAND SANITIZER

Manufacturer: Natuzen Co.,Ltd.
Effective date: 2020-03-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:39:02

Label at a glance#

ProductATOREN PREMIUM HAND SANITIZER

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

Uses: Hand sanitizer to help reduce bacteria on the skin

Dosage and administration

Directions: • Put enough product in your palm to cover hands and rub hands together briskly until dry. • Children under 6 years of age should be supervised when using. Not recommended for infants.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Ethyl alcohol 70%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Butylene Glycol, Aloe Extract(09), Water, Carbomer, Triethanolamine

PURPOSE

OTC - PURPOSE SECTION

Purpose: Hand Sanitizer

WARNINGS

WARNINGS SECTION

Warnings:

• Flammable. Keep away from fire or flame.
• For external use only.
• When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation or rash appears and lasts.
• Keep Out of Reach of Children.
• Do not eat.
• If swallowed, get medical help or contact a Poison Control
Center right away

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Uses

INDICATIONS & USAGE SECTION

Uses:
Hand sanitizer to help reduce bacteria on the skin

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:
• Put enough product in your palm to cover hands and rub
hands together briskly until dry.
• Children under 6 years of age should be supervised when
using. Not recommended for infants.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

ATOREN PREMIUM HAND SANITIZER
ALCOHOL
Water
Butylene Glycol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70930-107	70930-107-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
Water	059QF0KO0R	IACT
Butylene Glycol	3XUS85K0RA	IACT

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
093811cb-cb57-4ed1-8cce-a728f815350c			f32ea2ae-3dbc-4c85-8181-3013fc6dec7b	2024-04-19	Warnings	Exact identifier spl set id: f32ea2ae-3dbc-4c85-8181-3013fc6dec7b

Reported adverse events (FAERS/openFDA)#

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