Walmart

Manufacturer: Walmart Inc. | Medline Industries, LP
Effective date: 2024-09-18
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:19:45

Label at a glance#

ProductWalmart

Active ingredientISOPROPYL ALCOHOL

Label structure9 sections

Indications and uses

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

Dosage and administration

clean the affected area discard after a single use may be covered with a sterile bandage

Contacts and useful links#

PhoneLabel contact1-888-287-1915

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

do not get in the eyes or apply over large areas of the body
in case of deep or puncture wounds, animal bites or serious burns, consult a doctor
do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

the 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
discard after a single use
may be covered with a sterile bandage

Other information

OTHER SAFETY INFORMATION

do not flush
protect from freezing and avoid excessive heat
not made with natural rubber latex

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Manufacturing Information

SPL UNCLASSIFIED SECTION

Distributed by:

Walmart Inc.

702 SW 8th St, Bentonville, AR 72716 USA

Packaged in China with components from Taiwan

1-888-287-1915

REF: WAL090737EV2

REF: WAL45581RV2

V2 RH23LPD

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Blue Packet V2 RH23LPD

Box Blue V2 RH23LPD

Packet Red V2 RH23LPD

Box Red V2 RH23LPD

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797544	isopropyl alcohol 70 % Medicated Pad	PSN	4
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	4
797544	isopropyl alcohol 70 % Medicated Pad	SY	4
797544	isopropyl alcohol 70 % Topical Cloth	SY	4
797544	isopropyl alcohol 70 % Topical Swab	SY	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
49035-814-30	Walmart	1 in 1 PACKET	SWAB	1	4
49035-814-30	Walmart	100 in 1 BOX	SWAB	100	4
49035-814-60	Walmart	1 in 1 PACKET	SWAB	1	4
49035-814-60	Walmart	200 in 1 BOX	SWAB	200	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-814	WALMART (ISOPROPYL ALCOHOL) SWAB [WALMART INC.]	4	Current NDC, Legacy NDC, 4 package rows	20240920_d2b9f182-c341-c3b0-e053-2a95a90ac5a7.zip

Products#

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

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

Walmart
Isopropyl Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49035-814	49035-814-30, 49035-814-60

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
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

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
Walmart	ISOPROPYL ALCOHOL	Walmart Inc.	d2b9f182-c341-c3b0-e053-2a95a90ac5a7	2024-09-18	Warnings	Exact identifier ndc (package): 49035-814-60 ndc (package): 49035-814-30 ndc (product): 49035-814 ndc11 (package): 49035081460 ndc11 (package): 49035081430 spl id: 22655201-3f8c-b00b-e063-6294a90a80f1 spl set id: d2b9f182-c341-c3b0-e053-2a95a90ac5a7

Reported adverse events (FAERS/openFDA)#

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