everyone hand sanitizer ruby grapefruit

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 ruby grapefruit
Generic name: ETHYL ALCOHOL
Manufacturer: EO Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: aaed87bf-565f-41ad-ae40-66934428a1f8
SPL ID: 25b38846-971f-4b67-91ea-52e648e52dc2
Version: 6
Effective date: 2025-11-24
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:54:44

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		everyone hand sanitizer ruby grapefruit	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		EO Products, LLC	openfda.manufacturer_name
ndc	package	54748-604-08	openfda.package_ndc
ndc	package	54748-604-14	openfda.package_ndc
ndc	package	54748-604-09	openfda.package_ndc
ndc	package	54748-604-05	openfda.package_ndc
ndc	package	54748-604-17	openfda.package_ndc
ndc	package	54748-604-13	openfda.package_ndc
ndc	product	54748-604	openfda.product_ndc
ndc11	package	54748060408	derived:openfda.package_ndc
ndc11	package	54748060409	derived:openfda.package_ndc
ndc11	package	54748060405	derived:openfda.package_ndc
ndc11	package	54748060413	derived:openfda.package_ndc
ndc11	package	54748060417	derived:openfda.package_ndc
ndc11	package	54748060414	derived:openfda.package_ndc
rxcui		1020364	openfda.rxcui
spl id		25b38846-971f-4b67-91ea-52e648e52dc2	id
spl set id		aaed87bf-565f-41ad-ae40-66934428a1f8	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/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.