HYPERTONIC SALINE injection, solution

Hypertonic Saline by

Drug Labeling and Warnings

Hypertonic Saline by is a Animal medication manufactured, distributed, or labeled by Phoenix, 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 pre-
servatives. 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.

VETERINARY INDICATIONS

FOR ANIMAL USE ONLY

WARNINGS AND PRECAUTIONS

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 and 86°F)

GENERAL PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS

Manufactured by
Nova-Tech, Inc.
Grand Island, NE 68801

RMS 92-548

18-806-60

Rev. 06-10

NDC: 57319-554-08

Sterile - Preservative Free

Net Contents: 1000 mL

Manufactured for:
Clipper Distributing Company, LLC
St. Joseph, MO 64507

Trademarks are property of
Clipper Distributing Company, LLC

Lot No.

Exp. Date

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HYPERTONIC SALINE 
hypertonic saline injection, solution

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 57319-554
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: 57319-554-08	1000 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/16/2018

Labeler - Phoenix (150711039)

Registrant - Phoenix (150711039)

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