Label: ELECTROLYTE SOLUTION WITH DEXTROSE- dexolyte injection, solution
- NDC Code(s): 11695-6413-1, 11695-6413-5
- Packager: Covetrus
- Category: PRESCRIPTION ANIMAL DRUG LABEL
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Drug Label Information
Updated December 2, 2019
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- INDICATIONS:
- CONTRAINDICATIONS:
- CAUTION:
-
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 mLAdult 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. - PRECAUTIONS
- INFORMATION FOR OWNERS/CAREGIVERS
- VETERINARY INDICATIONS
- WARNINGS AND PRECAUTIONS
- Caution:
-
COMPOSITION:
Each 500 mL of sterile aqueous
solution contains:
Dextrose . H2O.........................12.50 gSorbitol...................................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
- STORAGE AND HANDLING
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ELECTROLYTE SOLUTION WITH DEXTROSE
dexolyte injection, solutionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:11695-6413 Route of Administration INTRAVENOUS, INTRAPERITONEAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dextrose Monohydrate (UNII: LX22YL083G) (Anhydrous Dextrose - UNII:5SL0G7R0OK) Dextrose Monohydrate 12.50 g in 500 mL Sorbitol (UNII: 506T60A25R) (Sorbitol - UNII:506T60A25R) Sorbitol 12.50 in 500 mL Sodium Lactate (UNII: TU7HW0W0QT) (Sodium Cation - UNII:LYR4M0NH37) Sodium Lactate 3.95 in 500 mL Sodium Chloride (UNII: 451W47IQ8X) (Chloride Ion - UNII:Q32ZN48698) Sodium Chloride 2.40 in 500 mL Potassium Chloride (UNII: 660YQ98I10) (Potassium Cation - UNII:295O53K152) Potassium Chloride 0.37 in 500 mL Magnesium Chloride (UNII: 02F3473H9O) (Magnesium Cation - UNII:T6V3LHY838) Magnesium Chloride 0.21 in 500 mL Calcium Chloride (UNII: M4I0D6VV5M) (Calcium Cation - UNII:2M83C4R6ZB) Calcium Chloride 0.19 in 500 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11695-6413-5 500 mL in 1 BOTTLE, PLASTIC 2 NDC:11695-6413-1 1000 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/2016 Labeler - Covetrus (603750329) Registrant - Nova-Tech, Inc. (196078976) Establishment Name Address ID/FEI Business Operations Nova-Tech, Inc. 196078976 manufacture, api manufacture
