MANNITOL 20%- mannitol injection 
Neogen Corporation

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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NeogenVet
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 m0smols/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.

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

RMS 92-384

Made in the USA

Item No. 09061

NDC 59051-8061-5

Mannitol Injection 20%

Sterile Solution

NeogenVet

Net Contentes: 100 mL

Lot No.

Exp. Date:

Neogen

Manufactured by: Nova-Tech, Grand Island, NE 68801

Manufactured for: Neogen Corporation, Lexington, KY 40511

859-254-1221

animalsafety.neogen.com

L566-0518

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

Mannitol Injection 20%

Mannitol Injection 20%

MANNITOL 20% 
mannitol injection
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:59051-8061
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:59051-8061-5100 mL in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/20/2011
Labeler - Neogen Corporation (042125879)
Registrant - Nova-Tech, Inc (196078976)
Establishment
NameAddressID/FEIBusiness Operations
Nova-Tech, Inc196078976manufacture

Revised: 11/2019
Document Id: 3143095a-8aa9-45f9-b84e-f69b3f404e70
Set id: 83deb341-d3b1-4417-98ee-b5ea850d86fa
Version: 1
Effective Time: 20191122
 
Neogen Corporation