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 Family Dollar Stores, 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

Warnings:

For medical emergencies, please seek profesisonal help. In case of deep or puncture wounds, or serious burns, consult a physician. If irritation or redness develops or persists, discontinue use and consult your healthcare provider.

Manufacturing information

Distributed by: Midwood Brands, LLC

500 Volvo Parkway, Chesapeake, VA 23320 USA

Made in India

Ref: FMD903968V1

V1 RK24PHX

Package Label

INGREDIENTS AND APPEARANCE

ALCOHOL PREP PADS 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55319-821
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: 55319-821-30	100 in 1 BOX	08/01/2024
1		1 in 1 PACKET
1		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	08/01/2024

Labeler - Family Dollar Stores, Inc. (024472631)

Registrant - Medline Industries, LP (025460908)