CALCIUM GLUCONATE injection, solution

Calcium Gluconate by

Drug Labeling and Warnings

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

Drug Details [pdf]

Each 100 mL CONTAINS:

Calcium Gluconate
(provides 2.14 grams Calcium) ...... 23 grams
Water For Injection................................q.s.

INACTIVE INGREDIENT

Contains boric acid as a solubilizing agent.
Electrolytes per 1000 mL: Calcium 1069 mEq;
Hypertonic

STORAGE AND HANDLING

Store at controlled room temperature 15 degrees C - 30 degrees C (59 degrees F - 86 degrees F).

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INFORMATION FOR OWNERS/CAREGIVERS

IBA STOCK # 494304

09NT6          Rev. 03-14        18-802

RMS 92-555

(calcium gluconate 23% solution)

NET CONTENTS: 500 mL

MANUFACTURED FOR:
IBA INC.
ANIMAL HEALTH DIVISION
27 PROVIDENCE RD.
MILLBURY, MA 01527

LOT NO.:                EXP. DATE:

INDICATIONS:

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

GENERAL PRECAUTIONS

FOR ANIMAL USE ONLY

DOSAGE AND ADMINISTRATION:

Cattle: 250 to 500 mL

Administer intravenously or intraperitoneally. 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 improvement in the animal's condition within 24 hours, consult a veterinarian.

GENERAL PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CALCIUM GLUCONATE 
calcium gluconate injection, solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 29983-2404
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: 29983-2404-1	500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/14/2014

Labeler - IBA Inc. (019494160)

Registrant - IBA Inc. (019494160)

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