Label: LACTATED RINGERS injection, solution
- NDC Code(s): 60270-132-20
- Packager: VetTek
- Category: PRESCRIPTION ANIMAL DRUG LABEL
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.
Updated November 8, 2019
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
DOSAGE AND ADMINISTRATION:
May be injected intravenously, subcutaneously or intraperitoneally (except in horses) using strict aseptic technique.
Cattle and Horses: 2 to 5 mL per pound of body weight depending on size and condition of animal, repeated 1 to 3 times daily or as needed.
Swine and Sheep: 2 to 5 mL per pound of body weight depending on size and condition of animal, repeated 1 to 3 times daily or as needed.
If administered subcutaneously divide the dosage into several sites of injection and massage points of injection to aid in absorption and help prevent inflammation and/or sloughing.
- STORAGE AND HANDLING
- INFORMATION FOR OWNERS/CAREGIVERS
Each 100 mL contains:
Sodium Chloride..................600 mg
Sodium Lactate...................310 mg
Potassium Chloride...............30 mg
Calcium Chloride Dihydrate....20 mg
Water for Injection...................q.s.
The Calcium, Potassium, Sodium, Chloride and Lactate contents are approximately 2.7, 4.0, 130, 109 and 28 mEq/liter, respectively.
Total Osmolar Concentration: 273 mOsm per liter (calculated).
Principal Display Panel
CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.
KEEP OUT OF REACH OF CHILDREN
FOR ANIMAL USE ONLY
Net Contents: 1000 mL (33.8 fl. oz)
Manufactured for: VetTek, Blue Springs, MO 64014
INGREDIENTS AND APPEARANCE
lactated ringers injection, solution
Product Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:60270-132 Route of Administration INTRAVENOUS, SUBCUTANEOUS, INTRAPERITONEAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 600 mg in 100 mL SODIUM LACTATE (UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) SODIUM LACTATE 310 mg in 100 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION 30 mg in 100 mL CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CHLORIDE 20 mg in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60270-132-20 1000 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/08/2019 Labeler - VetTek (056387798) Registrant - VetTek (056387798)