EO HAND SANITIZER Lavender

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: EO HAND SANITIZER Lavender
Generic name: ALCOHOL
Manufacturer: EO Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4192e27f-0034-4cd9-b9e0-27b52cb4b970
SPL ID: ddc684e2-ac67-4994-8ef3-099a2166c831
Version: 9
Effective date: 2025-11-21
Source export date: 2026-11-06
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/2026-11-06/3744b3ae389d13e8f30cade845ea29e0fc75bb043dcda980c2025693f0c10522/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 09:09:32

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		EO HAND SANITIZER Lavender	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		EO Products, LLC	openfda.manufacturer_name
ndc	package	54748-101-05	openfda.package_ndc
ndc	package	54748-101-01	openfda.package_ndc
ndc	package	54748-101-12	openfda.package_ndc
ndc	package	54748-101-02	openfda.package_ndc
ndc	package	54748-101-08	openfda.package_ndc
ndc	package	54748-101-09	openfda.package_ndc
ndc	product	54748-101	openfda.product_ndc
ndc11	package	54748010109	derived:openfda.package_ndc
ndc11	package	54748010105	derived:openfda.package_ndc
ndc11	package	54748010112	derived:openfda.package_ndc
ndc11	package	54748010108	derived:openfda.package_ndc
ndc11	package	54748010101	derived:openfda.package_ndc
ndc11	package	54748010102	derived:openfda.package_ndc
rxcui		1020364	openfda.rxcui
spl id		ddc684e2-ac67-4994-8ef3-099a2166c831	id
spl set id		4192e27f-0034-4cd9-b9e0-27b52cb4b970	set_id
unii		3K9958V90M	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: • Flammable, keep away from fire or flame. • For external use only. • Do not use in eyes. If contact occurs, flush thoroughly with water. • Stop use and contact a doctor if redness and irritation develops and persists for more than 72 hours. • Keep out of reach of children . If swallowed, get medical help or contact the Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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