MANNITOL- mannitol injection 
Covetrus

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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Covetrus
Mannitol

Recommended Use:

For use as an osmotic diuretic in dogs. 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.

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

NDC:11695-1254-1

Net contents: 100 mL (3.4 fl oz)

Lot No.

Exp. Date

Reorder #002469

Questions?

(855) 724-3461

Distributed by:

Covetrus North America

400 Metro Place North

Dublin, OH 43017

covetrus.com

Made in the USA

AH-002469-02

RMS-92-1192

L919-1119

REV: 1119

Caution:

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

FOR ANIMAL USE ONLY

KEEP OUT OF THE REACH OF CHILDREN

100 mL Label

MANNITOL 
mannitol injection
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:11695-1254
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:11695-1254-1100 mL in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/16/2020
Labeler - Covetrus (603750329)
Registrant - Nova-Tech, Inc (196078976)
Establishment
NameAddressID/FEIBusiness Operations
Nova-Tech, Inc196078976manufacture

Revised: 3/2020
Document Id: e935ba95-b3b5-4e3c-9689-3cece972a29c
Set id: 23594ac9-3b6b-4cd5-9e6c-9550ac1c73e4
Version: 1
Effective Time: 20200316
 
Covetrus