WALMART- isopropyl alcohol swab

Walmart by

Drug Labeling and Warnings

Walmart by is a Otc medication manufactured, distributed, or labeled by Walmart Inc., Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl alcohol 70% v/v

Purpose

first aid antiseptic

Uses

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

Warnings

For external use only.

Flammable, keep away from fire or flame.

When using this product

• 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 the condition persists or gets worse

Keep out of reach of children

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

Directions

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

Other information

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

Inactive ingredients

water

Other information

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

INGREDIENTS AND APPEARANCE

WALMART 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-278
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-278-10	100 in 1 BOX	10/01/2024
1		1 in 1 PACKET
1		5 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 79903-278-40	200 in 1 BOX	10/01/2024
2		1 in 1 PACKET
2		5 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/01/2024

Labeler - Walmart Inc. (051957769)

Registrant - Medline Industries, LP (025460908)