ISOPROPYL ALCOHOL 50 PERCENT- isopropyl alcohol liquid

Isopropyl alcohol by

Drug Labeling and Warnings

Isopropyl alcohol by is a Otc medication manufactured, distributed, or labeled by QUALITY CHOICE (Chain Drug Marketing Association). Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (by volume)

Isopropyl alcohol (50% conc.)

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
• if taken internally serious gastric disturbances will result

Ask a doctor before use if you have

• deep or puncture woods, 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 one week unless directed by a doctor

Stop use and ask a doctor if

• condition persists or gets worse

Keep out of reach of children.

In case of ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

• clean affected area
• apply small amount of this product on the area 1-3 times daily
• if bandaged, let dry first
• may be covered with a sterile bandage

Other information

• store at room temperature
• does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive ingredient

purified water

Questions or comments?

Call 1-248-449-9300 Monday-Friday 9AM-5PM EST

Principal Display Panel

Isopropyl

50% Rubbing Alcohol

First Aid antiseptic

Rubbing

Massaging

Sponge Bath

WARNING: FLAMMABLE, KEEP AWAY FROM SPARK, HEAT, OR FLAME.

FL OZ (mL)

TAMPER EVIDENT: DO NOT USE IF THE UNDER CAP PRINTED SAFETY FOIL IS BROKEN OR MISSING.

Distributed by C.D.M.A., Inc.©

43157 W. Nine Mile

Novi, MI 48376-0995

www.qualitychoice.com 

Package Label

Quality Choice Isopropyl 50 % Rubbing Alcohol

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL  50 PERCENT
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-939
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	50 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: 63868-939-12	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/30/2014	12/30/2021
2	NDC: 63868-939-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/30/2014	12/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	06/30/2014	12/30/2021

Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774)