EasyTouch Alcohol Prep Pads Sterile

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: EasyTouch Alcohol Prep Pads Sterile
Generic name: ISOPROPYL ALCOHOL
Manufacturer: MHC Medical Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: fd60ad34-5fd9-4440-9f3f-23beffc19dd9
SPL ID: e49b20ff-9ac0-45b4-94cf-b5fc61c4136d
Version: 9
Effective date: 2025-10-24
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:45

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		EasyTouch Alcohol Prep Pads Sterile	openfda.brand_name
generic name		ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		MHC Medical Products, LLC	openfda.manufacturer_name
ndc	package	42423-271-12	openfda.package_ndc
ndc	package	42423-271-04	openfda.package_ndc
ndc	package	42423-271-02	openfda.package_ndc
ndc	package	42423-271-01	openfda.package_ndc
ndc	product	42423-271	openfda.product_ndc
ndc11	package	42423027104	derived:openfda.package_ndc
ndc11	package	42423027101	derived:openfda.package_ndc
ndc11	package	42423027112	derived:openfda.package_ndc
ndc11	package	42423027102	derived:openfda.package_ndc
rxcui		797544	openfda.rxcui
spl id		e49b20ff-9ac0-45b4-94cf-b5fc61c4136d	id
spl set id		fd60ad34-5fd9-4440-9f3f-23beffc19dd9	set_id
unii		ND2M416302	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 fire or flame. Do not use with electrocautery procedures, or in/near eyes. Stop use if irritation or redness develops. If irritating condition persists for more than 72 hours, consult a physician. Keep out of reach of children . If swallowed, seek medical attention and/or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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