MANNITOL 20%- mannitol injection 
Clipper

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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Phoenix
MANNITOL Injection 20%

INDICATIONS:

Mannitol Injection 20% is indicated for use as an osmotic diuretic in canine species. Mannitol is essentially inert metabolically. When given parenterally, it is freely filtered at the glomerulus which produces osmotic diuresis as more than 90% of the mannitol injected escapes reabsorption.

Each 100 mL Contains:

Mannitol USP...................................20 g

Water for Injection...........................q.s.

This solution contains 1098 mOsmols/Liter

Dosage and Administration:

The usual canine dosage administered intravenously is 1.5 - 2.0 g per Kg body weight given over a 30 minute period. This is approximately 3.4-4.5 mL/lb of body weight.

Note:

Crystals of mannitol may form in a 20% saturated solution of mannitol. Dissolve the crystals by warming in hot water or autoclaving for 15 minutes. Cool to body temperature before administering. This is a single dose vial that contains no preservatives. Use entire contents when first opened or resterilize by autoclaving.

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

Manufactured by: Nova-Tech, Inc. Grand Island, NE 68801 for Neogen Corporation

Item No. 09061

1072-022114

Lot No.:

Exp. Date

NDC: 57319-521-05

Mannitol Injection 20%

Sterile Solution

Net Contentes: 100 mL

PhoenixTM

Manufactured for:

Clipper Distributing Company, LLC.

St. Joseph, MO 64507

Trademares are property of Clipper Distributing Company, LLC

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

Take Time Observe Label Directions

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

MANNITOL 20%

Mannitol 20%

MANNITOL 20% 
mannitol injection
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:57319-521
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MANNITOL (UNII: 3OWL53L36A) (MANNITOL - UNII:3OWL53L36A) MANNITOL20 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57319-521-05100 mL in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/27/2011
Labeler - Clipper (150711039)
Registrant - Nova-Tech, Inc (196078976)
Establishment
NameAddressID/FEIBusiness Operations
Nova-Tech, Inc196078976manufacture

Revised: 11/2019
Document Id: 7362d9a6-197c-4f19-aae3-3d0e958c4fdd
Set id: 1186453e-ffce-4b5c-90c2-3369ff5b4a79
Version: 1
Effective Time: 20191122
 
Clipper