FDA.reportPublic FDA data

Hand Wash

Manufacturer
Harmon Stores, Inc | Consumer Product Partners, LLC
Effective date
2024-09-19
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 20:54:38

Label at a glance#

ProductHand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

warnings

WARNINGS SECTION

For external use only: hands only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes.  If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops
  • condition persists 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 Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, fragrance, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, red 4, yellow 5

SPL UNCLASSIFIED SECTION

Distributed by Harmon Stores, Inc

650 Liberty Ave Union, NJ 07083 USA

Harmon Stores, Inc.

Visit us at www.facevalues.com

REFILL ONLY WITH FOAMING HAND SOAP, REGULAR LIQUID HAND SOAP WILL NOT FOAM.

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Helps Kill Harmful Germs

HARMON FACEVALUES

Antibacterial FOAMING HAND WASH

Gentle Enough for Everyday Use

7.5 FL OZ (221 mL)

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63940-46663940-466-96, 63940-466-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
GLYCERINPDC6A3C0OXIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM BENZOATEOJ245FE5EUIACT
FD&C RED NO. 4X3W0AM1JLXIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
2500aacc-6b9a-d4b3-e063-6394a90a4cd9cce754de-3b6d-443f-babf-641513636ec02024-10-21WarningsExact identifier
spl set id: cce754de-3b6d-443f-babf-641513636ec0

Reported adverse events (FAERS/openFDA)#

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