HYPERTONIC SALINE- hypertonic saline injection, solution 
Phoenix

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.

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Hypertonic Saline Solution 7.2%

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.

FOR ANIMAL USE ONLY

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.

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

TAKE TIME OBSERVE LABEL DIRECTIONS

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

label

HYPERTONIC SALINE 
hypertonic saline injection, solution
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:57319-554
Route of AdministrationINTRAVENOUS, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE7.2 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57319-554-081000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/16/2018
Labeler - Phoenix (150711039)
Registrant - Phoenix (150711039)
Establishment
NameAddressID/FEIBusiness Operations
Nova-Tech, Inc.196078976manufacture, api manufacture

Revised: 1/2018
Document Id: 2a6aa8a0-00a1-48a2-9153-adebe9b64c36
Set id: aaf0e81d-0923-40d9-b093-b64a14a92c8f
Version: 2
Effective Time: 20180129
 
Phoenix