Medi Fect Antiseptic Hand Wash

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: Medi Fect Antiseptic Hand Wash
Generic name: ETHYL ALCOHOL
Manufacturer: Medical Chemical Corporation
Product type: HUMAN OTC DRUG
SPL set ID: dc397d9c-9c12-41e5-ab7f-196fcad5bf97
SPL ID: 559190f3-0f95-df54-e063-6294a90a8199
Version: 17
Effective date: 2026-07-01
Source export date: 2026-11-06
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:03:49

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Medi Fect Antiseptic Hand Wash	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Medical Chemical Corporation	openfda.manufacturer_name
ndc	package	12745-177-06	openfda.package_ndc
ndc	package	12745-177-05	openfda.package_ndc
ndc	package	12745-177-04	openfda.package_ndc
ndc	package	12745-177-02	openfda.package_ndc
ndc	package	12745-177-08	openfda.package_ndc
ndc	package	12745-177-07	openfda.package_ndc
ndc	package	12745-177-03	openfda.package_ndc
ndc	package	12745-177-01	openfda.package_ndc
ndc	product	12745-177	openfda.product_ndc
ndc11	package	12745017708	derived:openfda.package_ndc
ndc11	package	12745017702	derived:openfda.package_ndc
ndc11	package	12745017701	derived:openfda.package_ndc
ndc11	package	12745017705	derived:openfda.package_ndc
ndc11	package	12745017706	derived:openfda.package_ndc
ndc11	package	12745017707	derived:openfda.package_ndc
ndc11	package	12745017704	derived:openfda.package_ndc
ndc11	package	12745017703	derived:openfda.package_ndc
spl id		559190f3-0f95-df54-e063-6294a90a8199	id
spl set id		dc397d9c-9c12-41e5-ab7f-196fcad5bf97	set_id
unii		3K9958V90M	openfda.unii
unii		H5RIZ3MPW4	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 no use in the eyes. Discontinue use if irritation or redness develops. Keep out of reach of children. In case of ingestion contact poison control center immediately.

Reported adverse events (FAERS/openFDA)#

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