ALCOHOL PREP PADS- isopropyl alcohol swab

Alcohol Prep Pads by

Drug Labeling and Warnings

Alcohol Prep Pads by is a Otc medication manufactured, distributed, or labeled by Topco Associates, Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl alcohol, 70% v/v

Purpose

Antiseptic

Uses

• For preparation of the skin prior to injection
• First aid antiseptic to help prevent infection in minor cuts, scrapes and burns.

Warnings

For external use only. Flammable, keep away from fire or flame.

Do not use

• With electrocautery procedures.
• Longer than one week unless directed by a physician.

When using this product

• Do not get in eyes.
• Do not apply over large areas of the body.
• In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

Stop use and ask a doctor if

• Irritation and redness develop.
• Condition gets worse or persists for more than 72 hours.

Keep out of reach of children

If accidentally swallowed, seek medical assistance or immediately contact a Poison Control Center.

Directions

• Apply to skin as needed.
• Discard after single use.

Other information

• Protect from freezing and avoid excessive heat.
• Not made with Natural Rubber Latex.

Inactive ingredients

water

Manufacturer information

DISTRIBUTED BY TOPCO ASSOCIATES LLC

ITASCA, IL 60143

©TOPCO MDLA1024

QUESTIONS? 1-888-423-0139

topcare@topco.com www.topcarebrand.com

PACKAGED IN CHINA WITH COMPONENTS FROM TAIWAN

REF TOP090734V2 V1 RK24SXM

Package label

INGREDIENTS AND APPEARANCE

ALCOHOL PREP PADS 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76162-808
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: 76162-808-30	100 in 1 BOX	12/05/2024
1		1 in 1 PACKET
1		0.5 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	12/05/2024

Labeler - Topco Associates (006935977)

Registrant - Medline Industries, LP (025460908)