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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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 WIH WATER AND CALL A PHYSICIAN. MAY CAUSE SKIN IRRITATION. AVOID CONTACT WITH EYES, SKIN, MUSCOUS MEMBRANES AND CLOTHING. WASH HANDS THOROUGHLY AFTER HANDLING.

WARNING! FLAMMABLE!

KEEP AWAY FROM HEAT AND OPEN FLAME.

STORAGE:

STORE AT CONTROLLED ROOM TEMPERATURE BETWEEN 15º - 30ºC (59º-86ºF). KEEP TIGHTLY CLOSED, PROTECT FROM LIGHT.

CONTENTS:

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

INACTIVE INGREDIENT

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.

Package/Label Principal Display Panel
NDC 30798-786-35
Durvet
70% Alcohol Solution
Contains 70% Isopropyl Alcohol
Rubefacient
www.durvet.com
NET CONTENTS: ONE GALLON (3.785 L)
Manufactured for:
Durvet, Inc.
Blue Springs, MO 64014
Iss 07-09

Bottle Label

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:30798-786
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: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: 03/2013
 
Durvet, Inc.