ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol solution

Isopropyl Rubbing Alcohol by

Drug Labeling and Warnings

Isopropyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by NDC, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

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
• 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

• 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 infected 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

PRINCIPAL DISPLAY PANEL 

REF: P907128

NDC: 43128-002-01

Isopropyl Rubbing
Alcohol 70% USP

Tamper evident cap for your protection.
If ring-band is detached from cap or missing do not use.

WARNING: Flammable

1 GAL ( 3785 mL )

Made in USA for:
NDC, Inc., 407 New Sanford Rd.
La Vergne, TN 37086
www.ProAdvantagebyNDC.com

Pro
ADVANTAGE®

by NDC

INGREDIENTS AND APPEARANCE

ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43128-002
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: 43128-002-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014
2	NDC: 43128-002-01	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014
3	NDC: 43128-002-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	06/01/2014

Labeler - NDC, Inc. (009831413)