FDA.reportPublic FDA data

Empire instant hand sanitizer

Manufacturer
EMPIRE MANAGED SOLUTIONS LLC
Effective date
2021-11-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:28:08

Label at a glance#

ProductEmpire instant hand sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

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

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Disinfectant

Uses

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

FLAMMABLE.
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.
Keep out of reach of children. If swallowed, seek medical advice or contact a Poison Control Center right away.

Direction

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.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Glycerin, Water, Aloe, Propylene Glycol, Butylene Glycol

Other information

SPL UNCLASSIFIED SECTION

Store between 15-30C (59-86F).

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63708-003-012023-10-30C16284748780-1e4f33bdf-9e52-d8a0-e053-dadaa90a6e4e7d439082-06a2-4864-9669-b8dbdc7afa24
63708-003-012022-07-29C16284748780-1e4f33bdf-9e52-d8a0-e053-dadaa90a6e4e7d439082-06a2-4864-9669-b8dbdc7afa24

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
63708-00363708-003-01

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
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALOEV5VD430YW9IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
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
08f52343-b275-3c16-e063-6294a90af9b37d439082-06a2-4864-9669-b8dbdc7afa242023-10-30WarningsExact identifier
spl set id: 7d439082-06a2-4864-9669-b8dbdc7afa24

Reported adverse events (FAERS/openFDA)#

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