FDA.reportPublic FDA data

Hand Sanitizer Solution 101

Manufacturer
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date
2025-12-23
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:28:26

Label at a glance#

ProductHand Sanitizer Solution 101
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For Hand Sanitizing to decrease bacteria on the skin.

Dosage and administration

Wash hands with soap and water. Rinse with potable water. Wet entire surface of hands with product especially the cuticles and fingernails. Rub hands together until dry. Do not rinse hands. Re-apply as needed.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride....0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Warnings

WARNINGS SECTION

For external use only.
Flammable keep away from fire or flame

When using this product

GENERAL PRECAUTIONS SECTION

Avoid contact with the eyes

In case of eye contact, flush eyes with water.

Stop use and ask doctor if

OTC - STOP USE SECTION

irritation or redness develops, if conditions persisit for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Conrol Center right away

Uses

INDICATIONS & USAGE SECTION

For Hand Sanitizing to decrease bacteria on the skin.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol

Directions

DOSAGE & ADMINISTRATION SECTION

Wash hands with soap and water. Rinse with potable water. Wet entire surface of hands with product especially the cuticles and fingernails. Rub hands together until dry. Do not rinse hands. Re-apply as needed.

Hand Sanitizer Solution 101

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50241-224-01Hand Sanitizer Solution 1013.67 kg in 1 BOTTLE, PLASTICLIQUID3.677
50241-224-02Hand Sanitizer Solution 1014 in 1 BOXLIQUID47
50241-224-08Hand Sanitizer Solution 101201.85 kg in 1 DRUMLIQUID201.857
50241-224-09Hand Sanitizer Solution 1011009.25 kg in 1 CONTAINERLIQUID1009.257

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50241-22450241-224-01, 50241-224-02, 50241-224-08, 50241-224-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT

Source Document#

Source XML · Source PDF

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
Hand Sanitizer Solution 101BENZALKONIUM CHLORIDEMorgan Gallacher Inc. DBA Custom Chemical Formulators Inc.81fa10d3-6dbb-4a72-bfff-2dd795f949682025-12-23WarningsExact identifier
ndc (package): 50241-224-02
ndc (package): 50241-224-01
ndc (package): 50241-224-09
ndc (package): 50241-224-08
ndc (product): 50241-224
ndc11 (package): 50241022402
ndc11 (package): 50241022401
ndc11 (package): 50241022408
ndc11 (package): 50241022409
spl id: 635a2612-04df-4dbb-b606-1c68c4179bd5
spl set id: 81fa10d3-6dbb-4a72-bfff-2dd795f94968

Reported adverse events (FAERS/openFDA)#

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