FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Vivier Pharma Inc.
Effective date
2022-10-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:50:30

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

For occasional and personal domestic use.

Dosage and administration

Rub thoroughly into hands for at least 30 seconds Allow to dry. • Supervise children when they use this product.

Label contents#

Full prescribing information#

Medicinal ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol – 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For occasional and personal domestic use.

Warnings

WARNINGS SECTION

For external use only. Flammability warning.
Keep away from open flame and sources of heat

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash or irritation develops and lasts.

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

  • Rub thoroughly into hands for at least 30 seconds
  • Allow to dry. • Supervise children when they use this product.

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature 15–30°C / 59–86°F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER/EAU, GLYCERIN, CARBOMER HOMOPOLYMER, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, TRIETHANOLAMINE, ALOE BARBADENSIS LEAF JUICE.

Questions?

OTC - QUESTIONS SECTION

1 877 484 8437

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67226-107767226-1077-1, 67226-1077-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB

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
081719c1-49e5-825f-e063-6294a90a70d3d5247b2a-9ec2-4073-a75c-c256d4a799662023-10-19WarningsExact identifier
spl set id: d5247b2a-9ec2-4073-a75c-c256d4a79966

Reported adverse events (FAERS/openFDA)#

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