ISOPROPYL ALCOHOL- isopropyl alcohol liquid 
Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

For Veterinary Use Only

Scrub hands and arms with soap and water, rinse with water, then scrub with alcohol solution for disinfecting.

External Solution for use as a topical antiseptic. may also be used for temporary relief of minor muscular aches or pain due to overexertion and fatigue. Apply full strength directly to affected area, wet thoroughly and massage briskly to stimulate circulation.

Store at controlled room temperature between 15° and 30°C (59°-86°F).

Manufactured by:
Ameri-Pac Inc.
St. Joseph, MO 64502

TAKE TIME OBSERVE LABEL DIRECTIONS

Trademarks are property of
Clipper Distributing Company, LLC

ACTIVE INGREDIENT

Isopropyl Alcohol ................ 70%

INERT INGREDIENT

Deionized Water ................. 30%
Total ................................. 100%

WARNING

For external use only. If taken internally, serious gastric disturbance will result. Avoid contact with eyes. In case of eye contact, flush thoroughly with water. Call a physician.

First Aid

Induce vomiting or use stomach pump.

CAUTION

FLAMMABLE
KEEP AWAY FROM FIRE OR FLAME

KEEP CONTAINER CLOSED WHEN NOT IN USE

Package/Label Principal Display Panel

NDC 57319-430-09

Isopropyl Alcohol 70%

FOR EXTERNAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

NET CONTENTS:
3.785 L (1 GALLON)

Phoenix Pharmaceutical, Inc.

Manufactured for:
Clipper Distributing Company, LLC
St. Joseph, MO 64507

Principal Display Panel - Bottle Label

Bottle Label

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57319-430
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:57319-430-22946 mL in 1 BOTTLE
2NDC:57319-430-093785 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other01/29/2002
Labeler - Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc. (150711039)

Revised: 03/2013
Document Id: 37755045-5a11-4115-926a-ffed60790e38
Set id: 37755045-5a11-4115-926a-ffed60790e38
Version: 1
Effective Time: 20130308
 
Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.