Walmart

Manufacturer: Walmart Inc. | Medline Industries, LP
Effective date: 2026-01-29
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:35:21

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 contact1-855-776-0662

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

OTC - STOP USE SECTION

if 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

Other information

SPL UNCLASSIFIED SECTION

This blood-related ReliOn product cannot be returned directly to a Walmart store, even unopened.

For questions, comments, or returns, please call 1-855-776-0662

DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716

PACKAGED IN CHINA WITH COMPONENTS FROM TAIWAN

*Sterility guaranteed unless individual wrapper is opened or damaged.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

box labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797544	isopropyl alcohol 70 % Medicated Pad	PSN	3
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	3
797544	isopropyl alcohol 70 % Medicated Pad	SY	3
797544	isopropyl alcohol 70 % Topical Cloth	SY	3
797544	isopropyl alcohol 70 % Topical Swab	SY	3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79903-278-10	Walmart	100 in 1 BOX	SWAB	100	3
79903-278-10	Walmart	1 in 1 PACKET	SWAB	1	3
79903-278-40	Walmart	1 in 1 PACKET	SWAB	1	3
79903-278-40	Walmart	200 in 1 BOX	SWAB	200	3

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
79903-278	79903-278-10, 79903-278-40

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

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.	1d75799d-081e-a38b-e063-6294a90adf35	2026-01-29	Warnings	Exact identifier ndc (package): 79903-278-40 ndc (package): 79903-278-10 ndc (product): 79903-278 ndc11 (package): 79903027810 ndc11 (package): 79903027840 spl id: 498c6920-3c46-9814-e063-6294a90a98ed spl set id: 1d75799d-081e-a38b-e063-6294a90adf35

Reported adverse events (FAERS/openFDA)#

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