HYPERTONIC SALINE- hypertonic saline injection, solution 
Animart

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 preservatives. Do not use if solution is not clear. 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.

Horses/Cattle: 50 to 100 mL per 100 lb body-weight one time. The specific 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.

Sterile - Preservative FREE

FOR ANIMAL USE ONLY

CAUTION:

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

KEEP OUT OF REACH OF CHILDREN

COMPOSITION:

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

Milliequivalents per liter

Cations
Sodium......................1232mEq/L
Anions
Chloride.....................1232 mEq/L
Total osmolarity is 2464 milliosmoles per liter.

Store between 15 degrees C - 30 degrees C (59 degrees F - 86 degrees F).

TAKE TIME OBSERVE LABEL DIRECTIONS

Net Contents: 1000 mL

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

18-806           Iss. 4-14

RMS# 92-1069

Lot No.           Exp. Date

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HYPERTONIC SALINE 
hypertonic saline injection, solution
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:23685-806
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:23685-806-601000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/09/201410/31/2020
Labeler - Animart (023151574)
Registrant - Animart (023151574)
Establishment
NameAddressID/FEIBusiness Operations
Nova-Tech, Inc.196078976manufacture

Revised: 11/2020
 
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