everyone Hand Sanitizer Coconut Lemon

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 Coconut Lemon
Generic name: ALCOHOL
Manufacturer: EO Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 16528009-90cf-46b8-9719-bdc6f435a191
SPL ID: ab3cc2a1-edbb-4284-b07b-8ae4f5331657
Version: 13
Effective date: 2025-11-27
Source export date: 2026-10-30
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/e37bebe0ee356110e46fe9b102632217cd5fd64caa93a64cf6ef0d92a0bfdb4c/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:50:06

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		everyone Hand Sanitizer Coconut Lemon	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		EO Products, LLC	openfda.manufacturer_name
ndc	package	54748-301-02	openfda.package_ndc
ndc	package	54748-301-12	openfda.package_ndc
ndc	package	54748-301-07	openfda.package_ndc
ndc	package	54748-301-05	openfda.package_ndc
ndc	package	54748-301-09	openfda.package_ndc
ndc	package	54748-301-13	openfda.package_ndc
ndc	package	54748-301-08	openfda.package_ndc
ndc	product	54748-301	openfda.product_ndc
ndc11	package	54748030112	derived:openfda.package_ndc
ndc11	package	54748030107	derived:openfda.package_ndc
ndc11	package	54748030113	derived:openfda.package_ndc
ndc11	package	54748030109	derived:openfda.package_ndc
ndc11	package	54748030102	derived:openfda.package_ndc
ndc11	package	54748030108	derived:openfda.package_ndc
ndc11	package	54748030105	derived:openfda.package_ndc
rxcui		1020364	openfda.rxcui
spl id		ab3cc2a1-edbb-4284-b07b-8ae4f5331657	id
spl set id		16528009-90cf-46b8-9719-bdc6f435a191	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.