SODIUM IODIDE- sodium iodide injection, solution 
Nova-Tech, Inc.

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%

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.

CAUTION

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

DOSAGE AND ADMINISTRATION:

Using aspetic 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.

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°C-30°C (59°F-86°F).

TAKE TIME OBSERVE LABEL DIRECTIONS

Manufactured by:

Nova-Tech, Inc.

Grand Island, NE 68801 USA

18-819

RMS 92-366

NDC# 65207-819-25

Net Contents:

250 mL (8.45 fl oz)

Assembled in USA

Lot No.

Exp. Date

250 mL label

SODIUM IODIDE 
sodium iodide injection, solution
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:65207-819
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION20 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65207-819-25250 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/22/2019
Labeler - Nova-Tech, Inc. (196078976)
Registrant - Nova-Tech, Inc. (196078976)
Establishment
NameAddressID/FEIBusiness Operations
Nova-Tech, Inc.196078976manufacture, api manufacture

Revised: 8/2019
Document Id: 8dfb9c1e-c6a0-47cc-89b1-b6fa57656f59
Set id: 259cce32-4dd0-4728-9976-8b1abf64e969
Version: 1
Effective Time: 20190822
 
Nova-Tech, Inc.