FDA.reportPublic FDA data

Alexander Hand Sanitizer

Manufacturer
Alexander Manufacturing Company
Effective date
2021-09-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:35:30

Label at a glance#

ProductAlexander Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin  • recommended for repeated use • for use when soap and water are not available.

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin 

• recommended for repeated use

• for use when soap and water are not available.

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame.

For external use only

Do not use

• in children less than 2 months of age.

• on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• wet hands thoroughly with product and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing

Other information

SPL UNCLASSIFIED SECTION

• store between 15-30° C (59-86° F)

• avoid freezing and excessive heat above 40° C (104° F)   

INACTIVE INGREDIENT SECTION

Inactive ingredients carbopol, diisopropylamine, glycerin, water.

OTC - QUESTIONS SECTION

Questions? +1-314-842-3344

You may also report serious side effects to this phone number.

Mon- Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

Antiseptic Hand Sanitizer

Made In USA

ALEXANDER

Packed by: Alexander Manufacturing Company 114 North Linoln Street, Towanda, IL 61776

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackagingPackagingPackagingPackaging

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78372-40278372-402-02, 78372-402-04, 78372-402-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
DIISOPROPYLAMINEBR9JLI40NOIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT

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
0123e220-e8ce-4fea-af28-888e08fb2c3cbebdd33b-8862-45ec-874e-60c717f51b012021-09-17WarningsExact identifier
spl id: 0123e220-e8ce-4fea-af28-888e08fb2c3c
spl set id: bebdd33b-8862-45ec-874e-60c717f51b01

Reported adverse events (FAERS/openFDA)#

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