MEDICHOICE ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

MediChoice Isopropyl Rubbing Alcohol by

Drug Labeling and Warnings

MediChoice Isopropyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by Owens & Minor Distribution, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl alcohol 70%

Purpose

First Aid Antiseptic

Uses

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, heat, spark, electrical. Flash point 72°F.
do not use with electrocautery procedures.

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 apply over large areas of the body do not use longer than 1 week unless directed by a doctor

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.

Directions

clean the affected area apply 1 to 3 times daily

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 ingredient

purified water

MediChoice Isopropyl Rubbing Alcohol, USP 4 FI.Oz./118mL (

39892-0500-1)

MediChoice Isopropyl Rubbing Alcohol, USP 16 FI.Oz./473mL (

39892-0500-2)

INGREDIENTS AND APPEARANCE

MEDICHOICE ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 39892-0500
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	700 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 39892-0500-1	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/20/2019
2	NDC: 39892-0500-2	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/20/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/20/2019

Labeler - Owens & Minor Distribution, Inc. (847412269)