FDA.reportPublic FDA data

Foaming Hand

Manufacturer
Intercon Chemical Co | Vi-Jon, LLC
Effective date
2022-08-26
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:54:59

Label at a glance#

ProductFoaming Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

wet hands apply pamlful 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

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

for external use only: hands

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 develop
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Rear label text

ADVERSE REACTIONS SECTION

DISTRIBUTED BY: INTERCON CHEMICAL CO.

1100 CENTRAL INDUSTRIAL DR.

ST. LOUIS, MO 63110

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ClearlyBetter

BY INTERCON

ANTIBACTERIAL

FOAMING

HAND SOAP

1150 mL (39 FL OZ)

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67502-224-452022-08-26C16284748780-1e4f33bdf-a0cd-d8a0-e053-dadaa90a6e4eClearly Better Foaming Hand Sanitizer 224.000/224AA
67502-224-452022-07-29C16284748780-1e4f33bdf-a0cd-d8a0-e053-dadaa90a6e4eClearly Better Foaming Hand Sanitizer 224.000/224AA

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
67502-22467502-224-45

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
GLYCERINPDC6A3C0OXIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
2a20f671-f4af-4703-a877-98ac57bcd173e2743583-23be-40d7-8fa6-f04b7fe92ae92023-09-25Warnings, Adverse reactionsExact identifier
spl set id: e2743583-23be-40d7-8fa6-f04b7fe92ae9

Reported adverse events (FAERS/openFDA)#

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