SODIUM IODIDE 20%- sodium iodide injection, solution 
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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Sodium Iodide 20% Injection

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 outside 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.

WARNING:

Not for use in lactating dairy cows.

CAUTION:

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

18-819-25

Iss. 04-12

RMS 92-1042

Lot No.

Exp. Date

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

CAUTION:

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

COMPOSITION:

Each 100 mL of sterile aqueous solution contains:

Sodium Iodide................20 grams

Water for injection...................q.s.

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

TAKE TIME OBSERVE LABEL DIRECTIONS

Trademarks are property of Clipper Distributing Company, LLC

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

Net Contents: 250 mL

Product Label

SODIUM IODIDE 20% 
sodium iodide injection, solution
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:57319-601
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION20 g  in 250 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57319-601-06250 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/01/2012
Labeler - Clipper (150711039)
Registrant - Clipper (150711039)
Establishment
NameAddressID/FEIBusiness Operations
Nova-Tech, Inc196078976manufacture, api manufacture

Revised: 5/2014
Document Id: 9dde79c3-8413-4b59-877b-4f144f1dc728
Set id: 68106ad8-882a-4933-971e-5a5855a4954c
Version: 1
Effective Time: 20140512
 
Clipper