DEXTROSE - dextrose monohydrate injection, solution 
Durvet

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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Dextrose 50%

Keep out of reach of children

ACTIVE INGREDIENTS:

Each 100 mL contains:

Dextrose . H2O .......................... 50 gms.

Water for Injection ........................... q.s.

DOSAGE AND ADMINISTRATION:

The usual dose is 50 mL per 100 lbs. of body weight.  It may be injected intravenously, intramuscularly, intraperitoneally or subcutaneously.  May be repeated in 8 to 10 hours or on successive days.  If administered intramuscularly or subcutaneously, the dosage should be divided among several locations and the point of injection massaged to aid in absorption.

NOTE:

If there is no noticeable improvement in the condition being treated after 3 or 4 days of treatment, consult your veterinarian.  Aseptic precaution should be observed such as using sterile needle and syringe.  Disinfect the site of injection.

CAUTION:

Solution should be warmed to body temperature and administered slowly.  This product contains no preservative.  Entire contents should be used upon entering.  Discard any unused portion.

INDICATIONS:

Dextrose 50% is indicated for the treatment of uncomplicated ketosis in cattle.

FOR USE IN ANIMALS ONLY

LIVESTOCK DRUG

Store between 15 degree C and 30 degree C (59 degree F and 86 degree F).

Take time.  Observe label directions.

image of container label

DEXTROSE 
dextrose injection, solution
Product Information
Product TypeOTC ANIMAL DRUG LABELItem Code (Source)NDC:30798-116
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR, INTRAPERITONEAL, SUBCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dextrose Monohydrate (ANHYDROUS DEXTROSE) Dextrose Monohydrate50 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30798-116-17500 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/26/2011
Labeler - Durvet (056387798)
Registrant - Durvet (056387798)

Revised: 11/2013
 
Durvet