Calcium Gluconate: Product Information

CALCIUM GLUCONATE- calcium gluconate injection, solution
Covetrus

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.

INDICATIONS:

For use as an aid in the treatment of hypocalcemia (parturient paresis, milk fever) in cattle.

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 strict aseptic conditions. If there is no apparent improvement in the animal’s condition within 24 hours, consult a veterinarian.

TAKE TIME OBSERVE LABEL DIRECTIONS

NDC 11695-5411-5

Calcium gluconate 23%

Calcium borogluconate solution

Volume: 16.907 fl oz (500 mL)

Questions? (855) 724-3461

Reorder #069167

18-802

RMS 92-1174

AH-069167-01

REV: 0719

Lot No.

Exp. Date

Distributed by:

Covetrus North America

400 Metro Place North

Dublin, OH 43017

covetrus.com

Manufactured by:

Nova-Tech Inc.

Grand Island, NE 68801

Assembled in USA

Composition:

Each 500 mL of sterile aqueous solution contains:

Calcium……………………………………..10.7 g

(as calcium borogluconate, equivalent to calcium gluconate, 23%)

Milliequivalents per liter

Cations

Calcium…………………………….1069 mEq/L

Anions

Gluconate………………………….1069 mEq/L

Store between 15°-30°C (59°-86°F).

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

500 mL label
(click image for full-size original)
500 mL label
(click image for full-size original)

CALCIUM GLUCONATE
calcium gluconate injection, solution
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:11695-6411
Route of Administration INTRAVENOUS, INTRAPERITONEAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CALCIUM GLUCONATE (CALCIUM CATION) CALCIUM GLUCONATE 23 g in 100 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:11695-6411-5 500 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 03/16/2020
Labeler — Covetrus (603750329)
Registrant — Nova-Tech, Inc. (196078976)
Establishment
Name Address ID/FEI Operations
Nova-Tech, Inc. 196078976 manufacture

Revised: 03/2020 Covetrus

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