H2One

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: H2One
Generic name: ETHYL ALCOHOL
Manufacturer: Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: a9bcecf7-7767-69b4-e053-2995a90a9247
SPL ID: 47afa270-3c4f-befe-e063-6394a90a3140
Version: 2
Effective date: 2026-01-05
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:17:14

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		M003	openfda.application_number
brand name		H2One	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	openfda.manufacturer_name
ndc	package	75742-006-05	openfda.package_ndc
ndc	package	75742-006-01	openfda.package_ndc
ndc	package	75742-006-04	openfda.package_ndc
ndc	package	75742-006-03	openfda.package_ndc
ndc	package	75742-006-02	openfda.package_ndc
ndc	product	75742-006	openfda.product_ndc
ndc11	package	75742000602	derived:openfda.package_ndc
ndc11	package	75742000601	derived:openfda.package_ndc
ndc11	package	75742000605	derived:openfda.package_ndc
ndc11	package	75742000604	derived:openfda.package_ndc
ndc11	package	75742000603	derived:openfda.package_ndc
rxcui		1305100	openfda.rxcui
spl id		47afa270-3c4f-befe-e063-6394a90a3140	id
spl set id		a9bcecf7-7767-69b4-e053-2995a90a9247	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 Avoid contact with eyes. If contact occurs, rinse thoroughly with water. FLAMMABLE, KEEP AWAY FROM FIRE Stop Use and Ask a Doctor Stop use and ask a doctor if rash or irritation or redness develops and lasts. Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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