Walgreens 70% Isopropyl Alcohol Wipes

Manufacturer: Walgreen Company | Kleen Test Products Corporation
Effective date: 2026-05-21
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: daily-update
Hydrated at: 2026-07-15 00:32:44

Label at a glance#

ProductWalgreens 70% Isopropyl Alcohol Wipes

Active ingredientISOPROPYL ALCOHOL

Label structure8 sections

Indications and uses

first aid to help prevent the risk of infection in: • minor cuts • scrapes • burns

Dosage and administration

• clean the affected area • apply product on the affected area of the body 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Contacts and useful links#

PhoneLabel contact1-800-925-4733

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in:
• minor cuts • scrapes • burns

Warnings

WARNINGS SECTION

For external use only.

Flammablekeep away from fire or flame, heat, spark, electrical

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

• deep or puncture wounds • animal bites •serious burns

When using this product

OTC - WHEN USING SECTION

• do not get in eyes • do not apply over large areas •do not use longer than 1 week unless directed by a doctor

Stop use and ask doctor if

OTC - STOP USE SECTION

condition persists or gets worse.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• clean the affected area • apply product on the affected area of the body 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Other information

SPL UNCLASSIFIED SECTION

• do not apply internally • keep canister tightly closed and stored at room temperature • hold away from face when opening

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-925-4733

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0311917143019	GTIN-13: 0311917143019 EAN-13: 0311917143019 GTIN-12: 311917143019 UPC-A: 311917143019 GTIN storage (14 digits): 00311917143019	Label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0363-6505-00	2024-01-30	C162847	48780-1	1030e365-1a6c-111a-e063-dadaa90a10e2	Walgreens 70% Isopropyl Alcohol Wipes
0363-6505-00	2024-01-30	C162847	48780-1	1030e365-1a6c-111a-e063-dadaa90a10e2	Walgreens 70% Isopropyl Alcohol Wipes

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Walgreens 70% Isopropyl Alcohol Wipes
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0363-6505	0363-6505-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
2	2026-02-19	full-release	2026-06-01 01:46:43

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens 70% Isopropyl Alcohol Wipes	ISOPROPYL ALCOHOL	Walgreen Company	e8b0ecc3-3a30-47c9-b7d1-518681d575b4	2026-05-21	Warnings	Exact identifier ndc (package): 0363-6505-00 ndc (product): 0363-6505 ndc11 (package): 00363650500 spl id: 5252be96-023c-7516-e063-6294a90a2329 spl set id: e8b0ecc3-3a30-47c9-b7d1-518681d575b4

Reported adverse events (FAERS/openFDA)#

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