Sodium Iodide: Product Information

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.

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
(click image for full-size original)

SODIUM IODIDE
sodium iodide injection, solution
Product Information
Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:65207-819
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM IODIDE (IODIDE ION) IODIDE ION 20 g in 100 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:65207-819-25 250 mL in 1 BOTTLE, PLASTIC None
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 Operations
Nova-Tech, Inc. 196078976 manufacture, api manufacture

Revised: 08/2019 Nova-Tech, Inc.

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