GUSTAR HAND SANITIZER (ETHANOL)

Manufacturer
GuStar Co Ltd | Pf Nature
Effective date
2020-05-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:29:07

Label at a glance#

ProductGUSTAR HAND SANITIZER (ETHANOL)
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin. Only when water and soap is not available.

Dosage and administration

■ Wet hands thoroughly with product and rub hands together until dry. ■ Supervise children under 6 years of age when using.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Dipropylene Glycol, Isoproply Myristate, Triethanolamine, Citrus Paradisi ( Grapefruit ) Seed Extract, Aloe Barbadensis Leaf Juice Powder

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

WARNINGS

WARNINGS SECTION

■ For external use only.
■ Flammable. ■ Keep away from heat and Flame.

When using this product
■ Keep out of eyes, ears and mouth.
■ If contact occurs, rinse eyes thoroughly with water.


Stop use and ask a doctor
■ If irritation and rash occurs.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ lf swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin. Only when water and soap is not available.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Wet hands thoroughly with product and rub hands together until dry.
■ Supervise children under 6 years of age when using.

Package Label: GUSTAR HAND SANITIZER 500mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

Package Label: GUSTAR HAND SANITIZER 60mL

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 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73819-000473819-0004-1, 73819-0004-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
e46f0d26-dbd0-eecd-e053-2995a90a0499a1983b42-8010-b0e6-e053-2a95a90a4c542022-07-22WarningsExact identifier
spl set id: a1983b42-8010-b0e6-e053-2a95a90a4c54

Reported adverse events (FAERS/openFDA)#

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