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:

57319-431-09Isopropyl Alcohol 99%ANTISEPTIC, DISINFECTANT RUBEFACIENT

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

Net Contents:

3.785 L (1 GAL)

PHOENIX

PHARMACEUTICAL, INC.

Manufactured for:

Clipper Distributing Company, LLC

St. Joseph, MO 64507

INDICATIONS:

For external use only as an antiseptic, disinfectant, and rubefacient.

TO MAKE A STANDARD SOLUTION (70%):

Dilute by adding 1 part water to 2 parts of this 99% Isopropyl Alcohol.

FOR EXTERNAL USE ONLY

DIRECTIONS:

Use full strength as topical antiseptic or for disinfections of instruments.

May be used for temporary relief of minor muscular aches or pain due to overexertion and fatigue. Apply full strength to affected area and massage briskly to stimulate circulation.

CAUTION:

In case of deep or puncture wounds or serious burns, consult a veterinarian. If redness, irritation, or swelling persists or increases, discontinue use and consult a veterinarian. Do not apply to irritated skin or if excessive irritation develops.

INGREDIENTS:

Isopropyl Alcohol ........... 99% w/v
Water ............................. q.s.

WARNING:

If taken internally, serious gastric disturbance will result.

First Aid:

Induce vomiting or use stomach pump. Call a physician immediately. Avoid getting into eyes or on mucous membranes. In case of eye contact, flush thoroughly with water. Call a physician immediately.

STORE AT CONTROLLED ROOM TEMPERATURE BETWEEN 15°-30°C (59°-86°F).

KEEP CONTAINER CLOSED WHEN NOT IN USE.

WARNING! FLAMMABLE! KEEP AWAY FROM HEAT AND OPEN FLAME.

TAKE TIME OBSERVE LABEL DIRECTIONS

Trademarks are property of
Clipper Distributing Company, LLC

Rev 1-10

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 57319-431
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	99 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: 57319-431-22	946 mL in 1 BOTTLE
2	NDC: 57319-431-09	3785 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		11/15/2002

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