Lite nFoamy E2 Sanitizing Handwash

Manufacturer
Spartan Chemical Company, Inc. | Spartan Chemical Company
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:38:12

Label at a glance#

ProductLite nFoamy E2 Sanitizing Handwash
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For hand washing 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 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 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 or 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.

Other Information

SPL UNCLASSIFIED SECTION

  • This product must be dispensed from an adequate dispenser located a sufficient distance from processing line to prevent accidental product contamination.
  • Do not contaminate water, food or feed by storage and disposal.

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 - Container Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Spartan®

Lite'nFoamy®

E2 Sanitizing
Handwash

Foam Sanitizing Handwash - Fragrance Free

  • For hand washing to decrease bacteria on the skin
  • Recommended for use by food service and food processing personnel

FOR INSTITUTIONAL AND INDUSTRIAL USE ONLY

See back panel for additional information.

Manufactured by
Spartan Chemical Company, Inc.

1110 Spartan Drive, Maumee, OH 43537 USA

Medical Emergency: 888-314-6171 / www.spartanchemical.com

Net Contents: 1 U.S. Gallon / 3.79 Liters

Principal Display Panel - Container Label
Principal Display Panel - Container Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN7
1493162Lite 'n Foamy 0.13 % Topical FoamPSN7
1493162benzalkonium chloride 1.3 MG/ML Topical Foam [Lite 'N Foamy]SBD7
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD7
1020365benzalkonium chloride 0.13 % Topical FoamSY7
1493162Lite 'N Foamy 0.13 % Topical FoamSY7

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130753727261161GTIN-13: 0753727261161
EAN-13: 0753727261161
GTIN-12: 753727261161
UPC-A: 753727261161
GTIN storage (14 digits): 00753727261161
lit01-0002-01.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64009-333-95Lite nFoamy E2 Sanitizing Handwash3.79 L in 1 CONTAINERSOAP3.797
64009-333-98Lite nFoamy E2 Sanitizing Handwash280.2 L in 1 CONTAINERSOAP280.27

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W71
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y1
Citric Acid MonohydrateINACTIVE INGREDIENT2968PHW8QP1
Cocamidopropylamine oxideINACTIVE INGREDIENTM4SL82J7HK1
Coco GlucosideINACTIVE INGREDIENTICS790225B1
Laurtrimonium chlorideINACTIVE INGREDIENTA81MSI0FIC1
WaterINACTIVE INGREDIENT059QF0KO0R1

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
64009-33364009-333-95, 64009-333-98

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62023-12-19full-release2026-06-01 00:05:02

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Citric Acid MonohydrateCITRIC ACID MONOHYDRATE2968PHW8QPSOAP / TOPICAL0.5 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
Citric Acid MonohydrateCITRIC ACID MONOHYDRATE2968PHW8QPSOAP / TOPICAL0.5 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
Citric Acid MonohydrateCITRIC ACID MONOHYDRATE2968PHW8QPSOAP / TOPICAL0.5 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates

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
Lite nFoamy E2 Sanitizing HandwashBENZALKONIUM CHLORIDESpartan Chemical Company, Inc.eb72b3ba-9cdd-40af-8e02-aa4b78ee02cc2025-10-07WarningsExact identifier
ndc (package): 64009-333-95
ndc (package): 64009-333-98
ndc (product): 64009-333
ndc11 (package): 64009033395
ndc11 (package): 64009033398
spl id: 4094e03d-6b68-262d-e063-6394a90a3001
spl set id: eb72b3ba-9cdd-40af-8e02-aa4b78ee02cc

Reported adverse events (FAERS/openFDA)#

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