ISOPROPYL ALCOHOL- isopropyl alcohol liquid 
Durvet, 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.

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Durvet 70% Alcohol Solution

NDC 30798-786-35
durvet
70% ALCOHOL SOLUTION
Contains 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

Label

Durvet 70 Alcohol Solution 3.785L

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:30798-786
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30798-786-353785 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other08/10/2009
Labeler - Durvet, Inc. (056387798)

Revised: 9/2013
Document Id: 3298361d-6579-42d4-90c7-778dbce23768
Set id: b1b9cfbb-1b46-414a-8a7b-efdb56edb36a
Version: 2
Effective Time: 20130920
 
Durvet, Inc.