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: ALCOHOL
Manufacturer: EO Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 045151b3-f08c-4e02-be33-00271e15b7f0
SPL ID: d1978147-6aad-4df7-a588-dd58b3798ff3
Version: 7
Effective date: 2025-11-27
Source export date: 2026-10-30
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/8d15bdc5962e7531569eaeb5b1b2e4919574d40a6782ab67345a27b890175a00/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:58:50

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 · 19 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		ALCOHOL	openfda.generic_name
manufacturer name		EO Products, LLC	openfda.manufacturer_name
ndc	package	54748-304-14	openfda.package_ndc
ndc	package	54748-304-05	openfda.package_ndc
ndc	package	54748-304-09	openfda.package_ndc
ndc	package	54748-304-13	openfda.package_ndc
ndc	package	54748-304-08	openfda.package_ndc
ndc	product	54748-304	openfda.product_ndc
ndc11	package	54748030414	derived:openfda.package_ndc
ndc11	package	54748030409	derived:openfda.package_ndc
ndc11	package	54748030405	derived:openfda.package_ndc
ndc11	package	54748030413	derived:openfda.package_ndc
ndc11	package	54748030408	derived:openfda.package_ndc
rxcui		1020364	openfda.rxcui
spl id		d1978147-6aad-4df7-a588-dd58b3798ff3	id
spl set id		045151b3-f08c-4e02-be33-00271e15b7f0	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 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.