CALCIUM GLUCONATE injection, solution

Calcium Gluconate by

Drug Labeling and Warnings

Calcium Gluconate by is a Animal medication manufactured, distributed, or labeled by Vedco, Nova-Tech, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS:

To be used as an
aid in the treatment of parturient
paresis (milk fever) in cattle.

DOSAGE AND ADMINISTRATION:

Cattle: 250 to 500 mL
Administer intravenously or intra-
peritoneally.Solution should be warmed to body
temperature and administered
slowly.  This product is sterile in
unopened container.  It contains
no preservative.  Use entire contents
when first opened.  It should be
handled under aseptic conditions. 
If there is no apparent improve-
ment in the animal's condition
within 24 hours, consult a veteri-
narian.

PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS

Distributed By
VEDCO, INC.
St. Joseph, MO 64507

VINV-CALC-500M
18-802              Rev. 09-15
RMS 92-364

Lot No.           Exp. Date

STERILE PRESERVATIVE FREE

NET CONTENTS: 500 mL (19.9 fl. oz.) 

ACTIVE INGREDIENT

Each 100 mL CONTAINS:

ACTIVE INGREDIENTS:

Calcium Gluconate (provides 2.14
grams Calcium) .............. 23 grams

INACTIVE INGREDIENTS:

Water for Injection ................... q.s.
Boric Acid
  (as solubilizing agent)...........3.5 grams
Electrolytes per 1000 mL: Calcium
1069 mEq;
Hypertonic                pH 2.5-4.5 

STORAGE AND HANDLING

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

GENERAL PRECAUTIONS

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CALCIUM GLUCONATE 
calcium gluconate injection, solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 50989-637
Route of Administration	INTRAVENOUS, INTRAPERITONEAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM GLUCONATE (UNII: SQE6VB453K) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM GLUCONATE	23 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50989-637-16	500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/14/2011

Labeler - Vedco (021634266)

Registrant - Vedco (021634266)

Establishment
Name	Address	ID/FEI	Business Operations
Nova-Tech, Inc.		196078976	manufacture, api manufacture