Green Island

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: Green Island
Generic name: ETHYL ALCOHOL
Manufacturer: Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: a7443a72-6ee5-07f7-e053-2995a90a3341
SPL ID: 47af97d6-ae83-adfe-e063-6394a90aa777
Version: 2
Effective date: 2026-01-05
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 18:52:38

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 · 30 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Green Island	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	openfda.manufacturer_name
ndc	package	75742-002-01	openfda.package_ndc
ndc	package	75742-002-04	openfda.package_ndc
ndc	package	75742-002-02	openfda.package_ndc
ndc	package	75742-002-10	openfda.package_ndc
ndc	package	75742-002-03	openfda.package_ndc
ndc	package	75742-002-06	openfda.package_ndc
ndc	package	75742-002-07	openfda.package_ndc
ndc	package	75742-002-05	openfda.package_ndc
ndc	package	75742-002-09	openfda.package_ndc
ndc	package	75742-002-08	openfda.package_ndc
ndc	package	75742-002-11	openfda.package_ndc
ndc	product	75742-002	openfda.product_ndc
ndc11	package	75742000203	derived:openfda.package_ndc
ndc11	package	75742000210	derived:openfda.package_ndc
ndc11	package	75742000202	derived:openfda.package_ndc
ndc11	package	75742000209	derived:openfda.package_ndc
ndc11	package	75742000211	derived:openfda.package_ndc
ndc11	package	75742000206	derived:openfda.package_ndc
ndc11	package	75742000205	derived:openfda.package_ndc
ndc11	package	75742000208	derived:openfda.package_ndc
ndc11	package	75742000207	derived:openfda.package_ndc
ndc11	package	75742000201	derived:openfda.package_ndc
ndc11	package	75742000204	derived:openfda.package_ndc
spl id		47af97d6-ae83-adfe-e063-6394a90aa777	id
spl set id		a7443a72-6ee5-07f7-e053-2995a90a3341	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 For external use only. Flammable, keep away from heat or flame Avoid contact with eyes or mouth. If irritation or redness & swelling occurs, discontinue use immediately. Do not use if you are allergic to alcohol Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.