FDA.reportPublic FDA data

Active Ingredients

Manufacturer
Spartan Chemical Company
Effective date
2026-07-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-07-21 05:10:18

Label at a glance#

ProductFoamyiQ Non-Alcohol Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

pump a small amount of foam into palm of hand rub thoroughly over all surfaces of both hands rub hands together briskly until dry

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

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 and redness develops, or if condition persists for more than 72 hours

keep out of reach of children. if swallowed, get medical help or contact a poison control center right away

Warnings

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

rub thoroughly over all surfaces of both hands

rub hands together briskly until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocomidopropyl PG-Dimonium Chloride Phosphate, Centimonium Chloride, Lautrimonium Chloride, Dihydroxyethyl cocamide oxide, citric acid, fragrance

Questions?

OTC - QUESTIONS SECTION

1-800-537-8990

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

iQ LabeliQ Label

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64009-22164009-221-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
FRAGRANCE 135765EM498GW35IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22023-12-19full-release2026-06-01 00:05:02

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
FoamyiQ Non-Alcohol Hand SanitizerFOAMYIQ NON-ALCOHOL HAND SANITIZERSpartan Chemical Companyee8a2af2-0572-19b1-e053-2995a90a23ae2026-07-17WarningsExact identifier
ndc (package): 64009-221-06
ndc (product): 64009-221
ndc11 (package): 64009022106
spl id: 56cea4e7-c425-e6bd-e063-6394a90a498d
spl set id: ee8a2af2-0572-19b1-e053-2995a90a23ae

Reported adverse events (FAERS/openFDA)#

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