ISOPROPYL ALCOHOL liquid

Isopropyl Alcohol by

Drug Labeling and Warnings

Isopropyl Alcohol by is a Animal medication manufactured, distributed, or labeled by Durvet, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NDC:

30798-786-35durvet70% ALCOHOL SOLUTIONContains 70% Isopropyl Alcohol

Rubefacient

www.durvet.com

NET CONTENTS: ONE GALLON (3.785 L)

FOR ANIMAL USE ONLY

INDICATIONS: Helps relieve minor muscular aches due to overexertion.

DIRECTIONS: Apply liberally and rub in.

CAUTION:

Harmful if swallowed.

WARNING:

FOR EXTERNAL USE ONLY.  Keep out of reach of children.  If taken internally, severe gastric disturbances will result.  In case of accidental ingestion, call a physician or poison control center immediately.  Causes eye irritation.  In case of contact, immediately flush eyes with water and call a physician.  May cause skin irritation.  Avoid contact with eyes, skin, mucous membranes and clothing.  Wash hands thoroughly after handling.

TAKE TIME OBSERVE LABEL DIRECTIONS

Manufactured for:

DURVET, INC.

Blue Springs, Missouri 64014

Iss. 07-09

KEEP OUT OF REACH OF CHILDREN

CONTENTS:

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

Purified Water .................... 30%

This preparation is made from Isopropyl Alcohol and does not contain, nor is it sold as a substitute for, ethyl or grain alcohol.

STORAGE:

Store at controlled room temperature between 15º - 30ºC (59º-86ºF).  Keep tightly closed, protect from light.

WARNING!  FLAMMABLE!

KEEP AWAY FROM HEAT AND OPEN FLAME

Lot No.          Exp. Date

DESCRIPTION

Label

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 30798-786
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: 30798-786-35	3785 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		08/10/2009

Labeler - Durvet, Inc. (056387798)