Label: DEXOLYTE- dextrose monohydrate, sorbitol, sodium lactate, sodium chloride, potassium chloride, magnesium chloride and calcium chloride injection, solution 

  • NDC Code(s): 57699-804-50
  • Packager: A & G Pharmaceuticals, Inc.
  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 03/13

If you are a consumer or patient please visit this version.

  • VETERINARY INDICATIONS

    FOR ANIMAL USE ONLY

    KEEP OUT OF REACH OF CHILDREN

    Close
  • CAUTION

    Federal law restricts this drug to use by or on the order of a licensed veterinarian.

    Close
  • INDICATIONS

    For use in conditions associated with fluid and electrolyte loss, such as dehydration, shock, vomiting and diarrhea, particularly when an immediate source of energy is also indicated.

    Close
  • CONTRAINDICATIONS

    Do not administer intraperitoneally to horses.

    Close
  • CAUTION

    This product contains no preservatives. Use entire contents when first opened. Discard any unused solution.

    Close
  • DOSAGE AND ADMINISTRATION

    Warm solution to body temperature and administer slowly (10 to 30 mL per minute) by intravenous or intraperitoneal injection, using strict aseptic procedures.

    Adult Cattle and Horses- 1000 to 2000 mL
    Calves, Ponies and Foals- 500 to 1000 mL
    Adult Sheep and Swine- 500 to 1000 mL

    These are suggested dosages. The actual amount and rate of fluid administration must be judged by the veterinarian in relation to the condition being treated and the clinical response of the animal, being careful to avoid overhydration.

    Close
  • COMPOSITION

    Each 500 mL of sterile aqueous solution contains:
    Dextrose.H2O...............................12.50 g
    Sorbitol........................................12.50 g
    Sodium Lactate..............................3.95 g
    Sodium Chloride.............................2.40 g
    Potassium Chloride.........................0.37 g
    Magnesium Chloride.6H2O..............0.21 g
    Calcium Chloride.2H2O...................0.19 g

    Milliequivalents per liter

    Cations
         Sodium..............................153 mEq/L
         Potassium.............................9 mEq/L
         Calcium.................................6 mEq/L
         Magnesium............................4 mEq/L

    Anions
         Chloride.............................101 mEq/L
         Lactate................................71 mEq/L
    Osmolarity (calc.) 602 mOsmol/L

    Close
  • STORAGE AND HANDLING

    Store between 15 degrees C - 30 degrees C (59 degrees F - 86 degrees F). Close
  • INFORMATION FOR OWNERS/CAREGIVERS

    Manufactured by:
    Nova-Tech, Inc.
    Grand Island, NE 68801
    Mfg. USA                 Iss. 06-09

    NET CONTENTS: 500 mL

    Manufactured for:
    A and G Pharmaceuticals
    Clarksburg, NJ 08510

    TAKE TIME OBSERVE LABEL DIRECTIONS

    Close
  • INGREDIENTS AND APPEARANCE
    DEXOLYTE 
    electrolyte with dextrose injection, solution
    Product Information
    Product Type PRESCRIPTION ANIMAL DRUG LABEL Item Code (Source) NDC:57699-804
    Route of Administration INTRAVENOUS, INTRAPERITONEAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Dextrose Monohydrate (ANHYDROUS DEXTROSE) Dextrose Monohydrate 12.50   in 500 mL
    Sorbitol (SORBITOL) Sorbitol 12.50   in 500 mL
    Sodium Lactate (LACTIC ACID) Sodium Lactate 3.95   in 500 mL
    Sodium Chloride (SODIUM CATION) Sodium Chloride 2.40   in 500 mL
    Potassium Chloride (POTASSIUM CATION) Potassium Chloride 0.37   in 500 mL
    Magnesium Chloride (MAGNESIUM CATION) Magnesium Chloride 0.21   in 500 mL
    Calcium Chloride (CALCIUM CATION) Calcium Chloride 0.19   in 500 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57699-804-50 500 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 01/28/2013
    Labeler - A & G Pharmaceuticals, Inc. (182147033)
    Registrant - A & G Pharmaceuticals, Inc. (182147033)
    Establishment
    Name Address ID/FEI Business Operations
    Nova-Tech, Inc. 196078976 manufacture
    Close