HYPERTONIC SALINE 7.2%- hypertonic saline injection, solution

Hypertonic Saline 7.2% by

Drug Labeling and Warnings

Hypertonic Saline 7.2% by is a Animal medication manufactured, distributed, or labeled by Covetrus, Nova-Tech, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Indications:

For use in replacement therapy of
sodium, chloride and water which may become
depleted in many diseases.

Caution:

This product contains no preservatives. Use
entire contents when first opened. Discard any
unused solution.

Dosage and Administration:

Warm to body temperature and administer slowly by intravenous or
subcutaneous injection. The amount and rate of
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.

GENERAL PRECAUTIONS

Sterile - Preservative Free

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

CAUTION:

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Composition:

Each 100 mL of sterile aqueous
solution contains:
Sodium chloride..........................7.2 g

Milliequivalents per liter

Cations
Sodium.............................1232 mEq/L
Anions
Chloride............................1232 mEq/L

Total osmolarity is 2464 milliosmoles per liter.

STORAGE AND HANDLING

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

PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS

Reorder #069179

Manufactured by:

Nova-Tech, Inc.

Grand Island, NE 68801

18-806
RMS 92-1178

NDC: 11695-6414-1

Volume: 33.814 fl oz (1000 mL)

Questions? (855) 724-3461

Distributed by:
Covetrus North America

400 Metro Place North

Dublin, OH 43017

covetrus.com

AH-069179-01
Rev: 0719

Lot No.    Exp. Date

Assembled in USA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HYPERTONIC SALINE 7.2% 
hypertonic saline injection, solution

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 11695-6414
Route of Administration	INTRAVENOUS, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	7.2 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11695-6414-1	1000 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/20/2019

Labeler - Covetrus (603750329)

Registrant - Covetrus (603750329)

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