Foaming Hand

Manufacturer
MORGAN GALLACHER INC
Effective date
2016-10-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:22:03

Label at a glance#

ProductFoaming Hand
Active ingredientCHLOROXYLENOL
Label structure10 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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Parachlorometaxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USES

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only

When Using this Product

OTC - WHEN USING SECTION

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

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or redness develops
or if condition persist

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help
or contact Posion Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to wet hands.
Work into a lather and rinse thoroughly.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Glycerine, Aloe Vera, DMDM Hydation, Fragrance, FD&C Yellow #5, FD&C Red #40

Foaming Hand Soap (Health Technologies)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50241-300-022022-12-29C16284748780-19d75b9d0-313f-f424-e053-dadaa90a57ceFoaming Hand Soap Health Technologies
50241-300-022020-01-31C16284748780-19d75b9d0-313f-f424-e053-dadaa90a57ceFoaming Hand Soap Health Technologies

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
50241-30050241-300-02

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
0d9df07b-bc9c-4eca-bb61-9bd9fa6b907430d03866-2f4c-48ff-b2ff-c9e301c36eb72022-12-29WarningsExact identifier
spl set id: 30d03866-2f4c-48ff-b2ff-c9e301c36eb7

Reported adverse events (FAERS/openFDA)#

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