MEDLINE ALCOHOL PREP- isopropyl alcohol swab

Medline Alcohol Prep by

Drug Labeling and Warnings

Medline Alcohol Prep by is a Otc medication manufactured, distributed, or labeled by 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 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

Manufacturing Information

www.medline.com

©2023 Medline Industries, LP

Made in China with Components from Taiwan

Manufactured for Medline Industries, LP

Three Lakes Drive, Northfield IL 60093 USA

1-800-MEDLINE

REF: MDS094550

Package Label

INGREDIENTS AND APPEARANCE

MEDLINE ALCOHOL PREP 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-812
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: 53329-812-09	1 in 1 PACKET	01/01/2021
1		2.3 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 53329-812-85	3996 in 1 CASE	01/01/2021
2		1 in 1 PACKET
2		2.3 mL in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 53329-812-86	3984 in 1 CASE	01/01/2021
3		1 in 1 PACKET
3		2.3 mL in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 53329-812-30	100 in 1 BOX	01/01/2021
4		1 in 1 PACKET
4		2.3 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	01/01/2021

Labeler - Medline Industries, LP (025460908)

Registrant - Medline Industries, LP (025460908)