INSTANT HAND SANITIZER WITH ALOE

Manufacturer
Ems Acquisition Corp.
Effective date
2022-11-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:49:11

Label at a glance#

ProductINSTANT HAND SANITIZER WITH ALOE 66.5% ETHYL ALCOHOL
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

for handwashing to decrease bacteria on skin without soap and water recommended for repeated use

Dosage and administration

wet hands and wrists thoroughly with product allow to dry without wiping children under 6 should be supervised while using this product

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66.5%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on skin without soap and water
  • recommended for repeated use

WARNINGS

WARNINGS SECTION

For external use only
Flammable. Keep away from fire or flame
Do not use in the eyes. If this happens, rinse thoroughly with water.
Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If ingested get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • wet hands and wrists thoroughly with product
  • allow to dry without wiping
  • children under 6 should be supervised while using this product

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

purified water, aloe vera, triethonolamine, carbomer, D&C blue #1, D&C yellow #10, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_EMS_Instant Hand Sanitizer01b LBL_EMS_Instant Hand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59228-50159228-501-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
2a4e46ad-bc65-f863-e063-6294a90a1fcceb5646ac-ad41-231b-e053-2995a90a8b432024-12-27WarningsExact identifier
spl set id: eb5646ac-ad41-231b-e053-2995a90a8b43

Reported adverse events (FAERS/openFDA)#

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