EMPIRE Hand Sanitizer

Manufacturer
EMPIRE MANAGED SOLUTIONS LLC | Guangzhou Zhongkebaishi Health Industry CO., LTD
Effective date
2022-01-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:13:33

Label at a glance#

ProductEMPIRE Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Apply product to hands. Rub hands briskly together until dry, ensuring full coverage of all areas of the hands including between the fingers. Children under 6 should be supervised when using this product.

Storage and handling

Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F). Product may discolor some fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. 

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Keep away from heat, flame or sparks.
This product is for external use only.
For use on hands only.
Do not use in or near the eyes. In case of eye contact rinse thoroughly with water.
Do not use on babies less than 2 months of age.
Do not use on open wounds.
Discontinue use if irritation or redness occurs.
If condition persists for more than 72 hours, consult a doctor.

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

Apply product to hands. Rub hands briskly together until dry, ensuring full coverage of all areas of the hands including between the fingers.
Children under 6 should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F).
Avoid freezing and excessive heat above 40C (104F).
Product may discolor some fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Glycerol, Triethanolamine, Water, Aloe Barbadensis Leaf Extract

Product Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
63708-00163708-001-01, 63708-001-02, 63708-001-03, 63708-001-04, 63708-001-05

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
d5f112d5-a337-dbaf-e053-2a95a90a6ce395b61463-97fc-4719-894d-d565cdc55dec2022-01-19WarningsExact identifier
spl id: d5f112d5-a337-dbaf-e053-2a95a90a6ce3
spl set id: 95b61463-97fc-4719-894d-d565cdc55dec

Reported adverse events (FAERS/openFDA)#

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