Walgreens

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: Walgreens
Generic name: ETHYL ALCOHOL
Manufacturer: Walgreens
Product type: HUMAN OTC DRUG
SPL set ID: ebf222f0-dc45-ee73-e053-2a95a90a0721
SPL ID: 51525a09-b43b-2edb-e063-6394a90a4509
Version: 6
Effective date: 2026-05-08
Source export date: 2026-11-06
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:36:28

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Walgreens	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Walgreens	openfda.manufacturer_name
ndc	package	0363-5721-02	openfda.package_ndc
ndc	product	0363-5721	openfda.product_ndc
ndc11	package	00363572102	derived:openfda.package_ndc
rxcui		581662	openfda.rxcui
spl id		51525a09-b43b-2edb-e063-6394a90a4509	id
spl set id		ebf222f0-dc45-ee73-e053-2a95a90a0721	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

For External use only : hands keep out of eyes, In case of contact with eyes, flush throughly with water. avoid contact with broken skin do not inhale or ingest. if irritation and redness develop condition persists for more than 72 hours. if swallowed , get medical help or contact a poision Control Centre right away.

Reported adverse events (FAERS/openFDA)#

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