ISOPROPYL ALCOHOL liquid

Isopropyl Alcohol by

Drug Labeling and Warnings

Isopropyl Alcohol 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%

Purpose

First Aid Antiseptic

Uses

For first aid to help prevent the risk of infection in minor:

• cuts
• scrapes
• burns

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Do not use

with electrocautery procedures. Use only in a well ventilated area; fumes may be toxic

When using this product do not

• get into eyes
• 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

condition persists or gets worse or lasts for more than 72 hours. Do not use longer than 1 week unless directed by a doctor.

Keep out of reach of children.

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

Directions

• Clean the affected area. Apply a small amount of the product on the area 1 to 3 times daily.
• May be covered with a sterile bandage.
• If bandaged, let dry first.

Other Information

• Does not contain, nor is intended as a substitute for grain or ethyl alcohol.
• Will produce serious gastric disturbances if taken internally.
• Protect from freezing and avoid excessive heat.

Inactive ingredients

Water

Package/Label Principal Display Panel

Medline

NDC: 53329-800-06

70%

Isopropyl Alcohol

First Aid Antiseptic

Warning

Flammable

Keep away from heat, spark, electrical fire of flame

Use only in a well-ventilated area; fumes can be harmful

16 FL OZ

(1 PT) 473 mL

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-800
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: 53329-800-06	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/16/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/16/2009

Labeler - Medline Industries, Inc. (025460908)