Everyone Hand Sanitizer Lavender Aloe

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: Everyone Hand Sanitizer Lavender Aloe
Generic name: ALCOHOL
Manufacturer: EO Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: d15c1fb9-b25b-45b8-a119-ee4c86c8d91c
SPL ID: 29f14ce4-cd16-4ffb-99c0-cb9ec5462ea3
Version: 9
Effective date: 2026-03-03
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:47:15

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Everyone Hand Sanitizer Lavender Aloe	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		EO Products, LLC	openfda.manufacturer_name
ndc	package	54748-303-02	openfda.package_ndc
ndc	package	54748-303-05	openfda.package_ndc
ndc	package	54748-303-09	openfda.package_ndc
ndc	package	54748-303-03	openfda.package_ndc
ndc	product	54748-303	openfda.product_ndc
ndc11	package	54748030305	derived:openfda.package_ndc
ndc11	package	54748030303	derived:openfda.package_ndc
ndc11	package	54748030309	derived:openfda.package_ndc
ndc11	package	54748030302	derived:openfda.package_ndc
rxcui		1020364	openfda.rxcui
spl id		29f14ce4-cd16-4ffb-99c0-cb9ec5462ea3	id
spl set id		d15c1fb9-b25b-45b8-a119-ee4c86c8d91c	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 ask a doctor if redness and irritation develop 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.