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: 36b26803-ed48-498f-bc0e-15473495a35a
SPL ID: b898dd5f-b908-4d52-b283-f0cd0bd1b8bd
Version: 11
Effective date: 2025-11-21
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:54:42

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 · 27 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	54748-201-10	openfda.package_ndc
ndc	package	54748-201-09	openfda.package_ndc
ndc	package	54748-201-03	openfda.package_ndc
ndc	package	54748-201-08	openfda.package_ndc
ndc	package	54748-201-04	openfda.package_ndc
ndc	package	54748-201-02	openfda.package_ndc
ndc	package	54748-201-05	openfda.package_ndc
ndc	package	54748-201-17	openfda.package_ndc
ndc	package	54748-201-07	openfda.package_ndc
ndc	product	54748-201	openfda.product_ndc
ndc11	package	54748020117	derived:openfda.package_ndc
ndc11	package	54748020110	derived:openfda.package_ndc
ndc11	package	54748020109	derived:openfda.package_ndc
ndc11	package	54748020108	derived:openfda.package_ndc
ndc11	package	54748020103	derived:openfda.package_ndc
ndc11	package	54748020102	derived:openfda.package_ndc
ndc11	package	54748020105	derived:openfda.package_ndc
ndc11	package	54748020104	derived:openfda.package_ndc
ndc11	package	54748020107	derived:openfda.package_ndc
rxcui		581660	openfda.rxcui
spl id		b898dd5f-b908-4d52-b283-f0cd0bd1b8bd	id
spl set id		36b26803-ed48-498f-bc0e-15473495a35a	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.