FDA.reportPublic FDA data

BENOA PREMIUM HAND SANITIZER

Manufacturer
Natuzen Co.,Ltd.
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:57

Label at a glance#

ProductBENOA PREMIUM HAND SANITIZER
Active ingredientALCOHOL
Label structure9 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:

Water, Butylene Glycol, Carbomer, Triethanolamine, PEG-60 Hydrogenated Castor Oil, Glycyrrhiza Uralensis (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Fragrance, Citral, Limonene

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.

Other information

OTHER SAFETY INFORMATION

Other information
• Store below 110’F (43’C)
• May discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70930-11070930-110-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
Water059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
PEG-60 Hydrogenated Castor Oil02NG325BQGIACT
GLYCYRRHIZA URALENSIS ROOT42B5YD8F0KIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ALOE VERA LEAFZY81Z83H0XIACT
CITRALT7EU0O9VPPIACT
LIMONENE, (+)-GFD7C86Q1WIACT

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
fa6e07d8-aaef-49ec-8a21-906bb4a63b36e7637863-d7dc-410b-9c18-82ab58ea27a42024-04-19WarningsExact identifier
spl set id: e7637863-d7dc-410b-9c18-82ab58ea27a4

Reported adverse events (FAERS/openFDA)#

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