DEXTROSE injection, solution

Dextrose by

Drug Labeling and Warnings

Dextrose by is a Animal medication manufactured, distributed, or labeled by Clipper, Nova-Tech, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE AND ADMINISTRATION:

For
intravenous administration only.

CAUTION:

Intravenous administration
must be done slowly and made under strict
aseptic conditions. Solution should be
warmed to body temperature prior to
administration. Cattle: 100 to 500 mL de-
pending on size and condition. Treatment
may be repeated in several hours or on
successive days as needed.

This is a single dose container. This pro-
duct contains no preservative. After a
quantity has been withdrawn for injection,
the remainder should be discarded. Do not
administer intraperitoneally.

GENERAL PRECAUTIONS

FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN

Each 100 mL contains:

Dextrose  H2O..............50 gms.

STORAGE AND HANDLING

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

INDICATIONS:

For use as an aid in
the treatment of acetonemia
(Ketosis) in cattle.

GENERAL PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS

RMS 92-540

18-801-50

Iss. 08-08

Lot No.

Exp. Date

Net Contents:
500 mL

Manufactured for:
Clipper Distributing Company, LLC
St. Joseph, MO 64507

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEXTROSE 
dextrose injection, solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 57319-543
Route of Administration	INTRAVENOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK)	DEXTROSE MONOHYDRATE	50 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57319-543-07	500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/14/2017

Labeler - Clipper (150711039)

Registrant - Clipper (150711039)

Establishment
Name	Address	ID/FEI	Business Operations
Nova-Tech, Inc.		196078976	manufacture, api manufacture