RESPONSIBLE HAND SANITIZER

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 22:33:50

Label at a glance#

ProductRESPONSIBLE HAND SANITIZER
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

Use: 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 fire or flame.

Do not use • on open skin wounds • on children under the age of 2 months

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

Advanced Moisturizing Formula with Vitamin E

Kills 99.99% of Germs

Made in PRC

Distributed by Clover Imaging Group

Hoffman Estates, IL 60169

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
76720-00376720-003-01, 76720-003-02, 76720-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
55295f56-26a9-4a28-9bbf-0fb50b9c46f46173746f-dae3-40f9-8d45-2e29283c52ef2022-07-13WarningsExact identifier
spl set id: 6173746f-dae3-40f9-8d45-2e29283c52ef

Reported adverse events (FAERS/openFDA)#

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