FDA.reportPublic FDA data

Foaming Antibacterial Hand - Intercon Chemical Company

Manufacturer
Intercon Chemical Company
Effective date
2026-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:36:53

Label at a glance#

ProductFoaming Antibacterial Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Pump a small amount of foam into palm of hand. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For hand washing to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of foam into palm of hand.
  • Scrub thoroughly for at least fifteen seconds.
  • Rinse completely and dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Phenoxyethanol, Fragrance, Citric Acid, Red 40, Blue 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label - 850 mL Cartridge_FrontPackage Label - 850 mL Cartridge_Front

Package Label - 850 mL Cartridge_BackPackage Label - 850 mL Cartridge_Back

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130789745002998GTIN-13: 0789745002998
EAN-13: 0789745002998
GTIN-12: 789745002998
UPC-A: 789745002998
GTIN storage (14 digits): 00789745002998		IFABHS_Back.jpg

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67502-11067502-110-85

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
FD&C BLUE NO. 1H3R47K3TBDIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
PHENOXYETHANOLHIE492ZZ3TIACT
FD&C RED NO. 40WZB9127XOAIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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 Antibacterial HandBENZALKONIUM CHLORIDEIntercon Chemical Company556b74d3-d37d-9508-e063-6294a90ae89f2026-06-29WarningsExact identifier
ndc (package): 67502-110-85
ndc (product): 67502-110
ndc11 (package): 67502011085
spl id: 556b504a-d5cf-3f02-e063-6394a90ae3b5
spl set id: 556b74d3-d37d-9508-e063-6294a90ae89f

Reported adverse events (FAERS/openFDA)#

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