SODIUM IODIDE injection, solution

Sodium Iodide by

Drug Labeling and Warnings

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

Drug Details [pdf]

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.

VETERINARY INDICATIONS

For Animal Use Only

WARNINGS

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.

STORAGE AND HANDLING

Store between 15°C-30°C (59°F-86°F).

WARNINGS AND PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SODIUM IODIDE 
sodium iodide injection, solution

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 65207-819
Route of Administration	INTRAVENOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	20 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65207-819-25	250 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/22/2019

Labeler - Nova-Tech, Inc. (196078976)

Registrant - Nova-Tech, Inc. (196078976)

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