FDA.reportPublic FDA data

Lite n Foamy Non-Alcohol Hand Sanitizer

Manufacturer
Spartan Chemical Company
Effective date
2023-12-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:05:02

Label at a glance#

ProductLite n Foamy Non-Alcohol Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

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 Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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, if condition persists for more than 72 hours consult a doctor.

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

Warnings Section

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, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Citric Acid, Fragrance

Questions?

OTC - QUESTIONS SECTION

1-800-537-8990

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

18oz Label18oz Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gallon LabelGallon Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN2
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD2
1038799benzalkonium chloride 0.1 % Topical FoamSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64009-222-82Lite n Foamy Non-Alcohol Hand Sanitizer532 g in 1 CONTAINERSOAP5322
64009-222-85Lite n Foamy Non-Alcohol Hand Sanitizer3790 g in 1 CONTAINERSOAP37902
64009-222-88Lite n Foamy Non-Alcohol Hand Sanitizer208200 g in 1 CONTAINERSOAP2082002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64009-222LITE N FOAMY NON-ALCOHOL HAND SANITIZER SOAP [SPARTAN CHEMICAL COMPANY]2Current NDC, Legacy NDC, 3 package rows20231220_ee8be683-f935-b32b-e053-2995a90aa51f.zip

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
64009-22264009-222-85, 64009-222-88, 64009-222-82

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
WATER059QF0KO0RIACT
FRAGRANCE 135765EM498GW35IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT

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
Lite n Foamy Non-Alcohol Hand SanitizerLITE N FOAMY NON-ALCOHOL HAND SANITIZERSpartan Chemical Companyee8be683-f935-b32b-e053-2995a90aa51f2023-12-19WarningsExact identifier
ndc (package): 64009-222-82
ndc (package): 64009-222-85
ndc (package): 64009-222-88
ndc (product): 64009-222
ndc11 (package): 64009022288
ndc11 (package): 64009022285
ndc11 (package): 64009022282
spl id: 0ce2595f-c940-021d-e063-6394a90ac4ad
spl set id: ee8be683-f935-b32b-e053-2995a90aa51f

Reported adverse events (FAERS/openFDA)#

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