FRESH HANDS FOAMING ANTIBACTERIAL HAND

Manufacturer
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date
2019-12-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:48:28

Label at a glance#

ProductFRESH HANDS FOAMING ANTIBACTERIAL HAND
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

-Apply to wet hands, work into a lather and rinse thoroughly. -Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride..............0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When Using this Product

GENERAL PRECAUTIONS SECTION

Avoid contact with the eyes.

In case of eye contact, flush eyes with water. Do not ingest.

Stop use and contact a doctor if irritation or redness develops

or if condition persist.

Keep out of reach of children.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

-Apply to wet hands, work into a lather and rinse thoroughly.

-Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl Betaine, Caprylyl Glucoside, Glycerine, Tetrasodium EDTA, Fragrance, Citric Acid, Aloe Vera, Benzisothiazol, Methylisothiozol, Yellow #5, Red #40

BUTLER FRESH HANDS FOAMING ANTIBACTERIAL HAND SOAP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BUTLER FRESH HANDS FOAMING ANTIBACTERIAL HAND SOAPimage descriptionimage description

Products#

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DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50241-99250241-992-01, 50241-992-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
aa8359c8-8adc-5c34-e053-2995a90a2e6db8d2d3cc-a42f-4da2-85ad-fb3134ae9e2f2020-07-15WarningsExact identifier
spl set id: b8d2d3cc-a42f-4da2-85ad-fb3134ae9e2f

Reported adverse events (FAERS/openFDA)#

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