Alcohol Disinfecting Wipe

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: Alcohol Disinfecting Wipe
Generic name: ALCOHOL
Manufacturer: McKesson Medical-Surgical
Product type: HUMAN OTC DRUG
SPL set ID: 64a0063d-a5da-4a46-9dca-16e4dbdac85c
SPL ID: 24382359-3128-c2ea-e063-6294a90ab1c6
Version: 5
Effective date: 2024-10-11
Source export date: 2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:37:31

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		Alcohol Disinfecting Wipe	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		McKesson Medical-Surgical	openfda.manufacturer_name
ndc	package	68599-5803-1	openfda.package_ndc
ndc	package	68599-5803-5	openfda.package_ndc
ndc	package	68599-5803-3	openfda.package_ndc
ndc	package	68599-5803-4	openfda.package_ndc
ndc	package	68599-5803-2	openfda.package_ndc
ndc	product	68599-5803	openfda.product_ndc
ndc11	package	68599580303	derived:openfda.package_ndc
ndc11	package	68599580301	derived:openfda.package_ndc
ndc11	package	68599580305	derived:openfda.package_ndc
ndc11	package	68599580304	derived:openfda.package_ndc
ndc11	package	68599580302	derived:openfda.package_ndc
rxcui		1489307	openfda.rxcui
spl id		24382359-3128-c2ea-e063-6294a90ab1c6	id
spl set id		64a0063d-a5da-4a46-9dca-16e4dbdac85c	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, flame or sources of ignition. For external use only. Do not use in or contact with eyes. Discontinue use if irritation and redness develop. If condition persists more than 72 hours, consult a doctor. Keep out of reach of children unless under adult supervision. If 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.