FDA.reportPublic FDA data

Active Ingredients

Manufacturer
Spartan Chemical Company, Inc. | Spartan Chemical Company
Effective date
2026-11-03
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
daily-update
Hydrated at
2026-11-06 02:02:52

Label at a glance#

ProductFoamyIQ Eucalyptus Mint Sanitizing Handwash
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand washing to decrease bacteria on the skin. Recommended tor repeated use.

Dosage and administration

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for 15 seconds. Rinse with potable water.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin.
  • Recommended tor repeated use.

Warnings

WARNINGS SECTION

  • For external use only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops, or if 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

  • Pump a small amount of foam into palm of hand.
  • Rub thoroughly over all surfaces of both hands for 15 seconds.
  • Rinse with potable water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid

Questions?

OTC - QUESTIONS SECTION

1-800-537-8990

Principal Display Panel - 1.25 L Container Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

foamy iQ™

EUCALYPTUS MINT
SANITIZING HANDWASH

#114603V02

Principal Display Panel - 1.25 L Container Label
Principal Display Panel - 1.25 L Container Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130753727264537GTIN-13: 0753727264537
EAN-13: 0753727264537
GTIN-12: 753727264537
UPC-A: 753727264537
GTIN storage (14 digits): 00753727264537		foa03-0002-01.jpg

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
64009-20164009-201-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCO GLUCOSIDEICS790225BIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CAPRYLYL/CAPRYL GLUCOSIDEE00JL9G9K0IACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72025-10-07full-release2026-06-01 01:38:08
62023-12-19full-release2026-06-01 00:04:57

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
4094a7d7-d7fd-fc9b-e063-6294a90aa2e46c78d527-cbca-429a-9ce3-13c392de707e2025-10-07WarningsExact identifier
spl set id: 6c78d527-cbca-429a-9ce3-13c392de707e

Reported adverse events (FAERS/openFDA)#

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