FDA.reportPublic FDA data

Foaming Hand

Manufacturer
Cintas Corporation | Nice-Pak Products, LLC
Effective date
2026-02-02
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:36:07

Label at a glance#

ProductFoaming Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

for handwashing to decrease bacteria on the skin

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

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

for external use only: hands only

Flammable, keep away from fire or flame.

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 and redness develop
  • 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

SPL UNCLASSIFIED SECTION

  • do not store above 105°F
  • may discolor some fabrics
  • harmful to wood finshes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, citric acid, tetrasodium EDTA, sodium benzoate

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Product is NSF certified for use as a hand sanitizer in and around food processing areas.

CiNTAS

800mL/27.0 FL OZ

Manufactured for Cintas Corp.

Mason, OH 45040

800-CINTAS1

NSF Nonfood Compounds Program

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAND

SOAP

ANTIBACTERIAL

FOAM

image descriptionimage descriptionimage descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42961-224-71Foaming Hand800 mL in 1 BOTTLE, PUMPLOTION8008

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42961-22442961-224-71

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
GLYCERINPDC6A3C0OXIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM BENZOATEOJ245FE5EUIACT
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
Foaming HandBENZALKONIUM CHLORIDECintas Corporation17fb34e7-c9e6-41aa-991f-bb54c84ed79c2026-02-02Warnings, Adverse reactionsExact identifier
ndc (package): 42961-224-71
ndc (product): 42961-224
ndc11 (package): 42961022471
spl id: 49dac8e8-231b-6f18-e063-6394a90aecd1
spl set id: 17fb34e7-c9e6-41aa-991f-bb54c84ed79c

Reported adverse events (FAERS/openFDA)#

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