ISOPROPYL ALCOHOL liquid

Isopropyl Alcohol by

Drug Labeling and Warnings

Isopropyl Alcohol by is a Animal medication manufactured, distributed, or labeled by Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NDC:

57319-430-09Isopropyl Alcohol 70%FOR EXTERNAL USE ONLYKEEP OUT OF REACH OF CHILDREN   

NET CONTENTS:

3.785L (1 GALLON)

PHOENIXTM

PHARMACEUTICAL, INC.

Manufactured for:

Clipper Distributing Company, LLC

St. Joseph, MO 64507

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

Rev. 10-09

TAKE TIME OBSERVE LABEL DIRECTIONS

Trademarks are property of
Clipper Distributing Company, LLC

ACTIVE INGREDIENT

ACTIVE INGREDIENT:

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

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 57319-430
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: 57319-430-22	946 mL in 1 BOTTLE
2	NDC: 57319-430-09	3785 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		01/29/2002

Labeler - Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc. (150711039)