FDA.reportPublic FDA data

foamyiQ LEMON BLOSSOM HAND SANITIZER

Manufacturer
Spartan Chemical Company
Effective date
2022-12-28
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:42:34

Label at a glance#

ProductFoamyIQ Lemon Blossom 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#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin.
  • Recommended for 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.
  • Rub hands together briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid, Fragrance

Questions?

OTC - QUESTIONS SECTION

1-800-537-8990

Principal Display Panel - 1.25 L Container Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

foamy iQ™

LEMON BLOSSOM
HAND SANITIZER

#114604V02

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

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64009-20264009-202-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCO GLUCOSIDEICS790225BIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
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
0e75e818-8de3-59e4-e063-6394a90a670468f7c748-403e-4de3-96ab-64a8d3aa33052024-01-08WarningsExact identifier
spl set id: 68f7c748-403e-4de3-96ab-64a8d3aa3305

Reported adverse events (FAERS/openFDA)#

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