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:

• Minor cuts
• scrapes
• burns

Warnings

For external use only.

Flammable. Keep away from fire or flame, heat, spark, electrical

Ask a doctor before use if you have

Deep or puncture wounds, animal bites or serious burns.

When using this product

• do not get into eyes
• Do not inhale
• Do not apply over large ares of the body
• Do not use longer than 1 week

Stop use and ask a doctor if condition persists or gets worse

Keep out of reach of children.

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

Caution

Fumes can be acutely irritating to skin, eyes, and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product

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.

Inactive ingredients

Water

Package Label

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-798
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: 53329-798-03	29.57 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2015
2	NDC: 53329-798-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2015
3	NDC: 53329-798-23	946.35 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2015
4	NDC: 53329-798-25	3790 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/30/2015

Labeler - Medline Industries, Inc. (025460908)

Establishment
Name	Address	ID/FEI	Business Operations
Hydrox Laboratories		025164302	manufacture(53329-798)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc.		088520668	manufacture(53329-798)