Lite nFoamy Eucalyptus Mint Sanitizing Handwash

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Lite nFoamy Eucalyptus Mint Sanitizing Handwash
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Spartan Chemical Company, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b464daa7-354a-4a6d-97aa-f77911aa5dc3
SPL ID: 4094bed1-f0f6-0a67-e063-6394a90ad4e7
Version: 8
Effective date: 2025-10-07
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:49

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Lite nFoamy Eucalyptus Mint Sanitizing Handwash	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Spartan Chemical Company, Inc.	openfda.manufacturer_name
ndc	package	64009-332-75	openfda.package_ndc
ndc	package	64009-332-78	openfda.package_ndc
ndc	package	64009-332-72	openfda.package_ndc
ndc	product	64009-332	openfda.product_ndc
ndc11	package	64009033278	derived:openfda.package_ndc
ndc11	package	64009033272	derived:openfda.package_ndc
ndc11	package	64009033275	derived:openfda.package_ndc
rxcui		1020365	openfda.rxcui
rxcui		1493162	openfda.rxcui
spl id		4094bed1-f0f6-0a67-e063-6394a90ad4e7	id
spl set id		b464daa7-354a-4a6d-97aa-f77911aa5dc3	set_id
unii		F5UM2KM3W7	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings 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.

Reported adverse events (FAERS/openFDA)#

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