FDA.reportPublic FDA data

First Safety

Manufacturer
General Printing & Design, Inc.
Effective date
2021-10-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:33:52

Label at a glance#

ProductFirst Safety
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information • Store between 59°-86°F (15°-30°C) • Avoid freezing and excessive heat above 104°F (40°C)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS SECTION

Warnings For external use only.

Flammable. Keep away from heat or flame.

Do not use • on open skin wounds

• in children less than 2 months of age

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

DOSAGE & ADMINISTRATION SECTION

Directions • Place enough product on hands to cover all surfaces. Rub hands together until dry.

• Supervise children under 6 years of age when using this product to avoid swallowing.

STORAGE AND HANDLING SECTION

Other information • Store between 59°-86°F (15°-30°C)

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

INACTIVE INGREDIENT SECTION

Inactive ingredients ​purified water, glycerin, triethanolamine, carbomer, vitamin E

SPL UNCLASSIFIED SECTION

Kills 99.9% of Germs

FIRST + SAFETY

45 BARTLETT STREET, MARLBOROUGH, MA 01752

www.firstsafetyco.com

800-258-2000

MADE IN CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

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
76720-00276720-002-01, 76720-002-02, 76720-002-03, 76720-002-04, 76720-002-05, 76720-002-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT

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
3f48b72f-cdb3-412b-829e-61921555caf3876ce6bc-84ff-4479-b495-4756eb9cfa0b2022-07-13WarningsExact identifier
spl set id: 876ce6bc-84ff-4479-b495-4756eb9cfa0b

Reported adverse events (FAERS/openFDA)#

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