Animal NDC 46066-819-25 Sodium Iodide 20%
Sodium Iodide

Animal Product Information

Field Name Field Value
Animal NDC Code 46066-819-25
Proprietary Name Sodium Iodide 20% What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Sodium Iodide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Labeler Name Aspen Veterinary
Product Type Prescription Animal Drug
Usage Information
    For use as an aid in the treatment ofactinomycosis (lumpy jaw), actinobacillosis(wooden tongue) and necrotic stomatitis incattle. 
Active Ingredient(s)
  • Sodium Iodide
Marketing Category UNAPPROVED DRUG OTHER What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Sodium Iodide 20% Images

Sodium Iodide 20% Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Indications:



For use as an aid in the treatment of
actinomycosis (lumpy jaw), actinobacillosis
(wooden tongue) and necrotic stomatitis in
cattle. 


Contraindications:



The use of sodium iodide is contraindicated in
pregnancy and hyperthyroidism. 


Dosage And Administration:



Using aseptic procedures, administer slowly by
intravenous injection. Inject carefully to avoid
deposition ouside of the vein. The usual dose
is 30 mg per pound of body weight (15 mL/100
lb). May be repeated at weekly intervals, if
necessary. 


Information For Owners/Caregivers



Distributed by:
Aspen Veterinary Resources, Ltd.
Liberty, MO 64068 USA              A247NT 05/15
www.aspenveterinaryresources.com

Manufactrued by:
Nova-Tech, Inc.
Grand Island, NE 68801 USA    18-819  RMS# 92-587

NET CONTENTS:
250 mL (8.45 fl oz)

Lot No.    Exp. Date 


Caution:



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

Animals vary in their susceptibility of iodides.
Administer with caution until the animal's
tolerance is determined. Discontinue treatment
if adverse reactions occur. 


Veterinary Indications



For Animal Use Only


Warnings



Keep Out of Reach of Children

TAKE TIME OBSERVE LABEL DIRECTIONS


Composition:



Each 100 mL of sterile aqueous solution
contains:
Sodium Iodide..............................20 grams
Water for Injection................................q.s. 


Warning:



Not for use in lactating dairy cows.


Storage And Handling



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


* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.