SODIUM IODIDE injection, solution

Sodium Iodide by

Drug Labeling and Warnings

Sodium Iodide by is a Animal medication manufactured, distributed, or labeled by AgriLabs, 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 suscep-
tibility 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 and 30°C (59°F and 86°F).

WARNINGS AND PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS

®Registered trademark of Agri Laboratories, Ltd.

Iss. 07-10

LOT

EXP

NDC: 57561-614-25

RMS 92-589

18-819-25

Manufactured for
Agri Laboratories, Ltd.
St. Joseph, MO 64503

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SODIUM IODIDE 
sodium iodide injection, solution

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 57561-614
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: 57561-614-25	250 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/16/2018

Labeler - AgriLabs (155594450)

Registrant - AgriLabs (155594450)

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