Sodium Iodide 20% Injection

Manufacturer
Aspen Veterinary | Nova-Tech, Inc
Effective date
2016-01-27
Label type
PRESCRIPTION ANIMAL DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:39:56

Label at a glance#

ProductSodium Iodide 20%
Active ingredientSODIUM IODIDE
Label structure13 sections

Dosage and administration

Using aseptic procedures, administer slowly by intravenous injection. Inject carefully to avoid deposition ouside 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. 

Storage and handling

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

Label contents#

Full prescribing information#

INDICATIONS:

INDICATIONS & USAGE SECTION

For use as an aid in the treatment of
actinomycosis (lumpy jaw), actinobacillosis
(wooden tongue) and necrotic stomatitis in
cattle. 

CONTRAINDICATIONS:

CONTRAINDICATIONS SECTION

The use of sodium iodide is contraindicated in
pregnancy and hyperthyroidism. 

DOSAGE AND ADMINISTRATION:

DOSAGE & ADMINISTRATION SECTION

Using aseptic procedures, administer slowly by
intravenous injection. Inject carefully to avoid
deposition ouside 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. 

INFORMATION FOR OWNERS/CAREGIVERS SECTION

Distributed by:
Aspen Veterinary Resources, Ltd.
Liberty, MO 64068 USA              A247NT 05/15
www.aspenveterinaryresources.com

Manufactrued by:
Nova-Tech, Inc.
Grand Island, NE 68801 USA    18-819  RMS# 92-587

NET CONTENTS:
250 mL (8.45 fl oz)

Lot No.    Exp. Date 

CAUTION:

PRECAUTIONS SECTION

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

VETERINARY INDICATIONS SECTION

For Animal Use Only

WARNINGS SECTION

Keep Out of Reach of Children

COMPOSITION:

DOSAGE FORMS & STRENGTHS SECTION

Each 100 mL of sterile aqueous solution
contains:
Sodium Iodide..............................20 grams
Water for Injection................................q.s. 

WARNING:

WARNINGS SECTION

Not for use in lactating dairy cows.

CAUTION:

PRECAUTIONS SECTION

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

STORAGE AND HANDLING SECTION

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

WARNINGS SECTION

TAKE TIME OBSERVE LABEL DIRECTIONS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
435151sodium iodide 20 % Injectable SolutionPSN6
435151sodium iodide 200 MG/ML Injectable SolutionSCD6
435151sodium iodide 20 % Injectable SolutionSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130099355001121GTIN-13: 0099355001121
EAN-13: 0099355001121
GTIN-12: 099355001121
UPC-A: 099355001121
GTIN storage (14 digits): 00099355001121
92-587.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
46066-819-25Sodium Iodide 20%250 mL in 1 BOTTLE, PLASTICINJECTION, SOLUTION2506

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
46066-819SODIUM IODIDE 20% (SODIUM IODIDE) INJECTION, SOLUTION [ASPEN VETERINARY]61 package rows20160127_a1e4f1ee-9c3c-4772-a8d0-d0c73acca5df.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Sodium IodideACTIVE INGREDIENTF5WR8N145C5
Iodide IonACTIVE MOIETY09G4I6V86Q5

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46066-81946066-819-25

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM IODIDEF5WR8N145CACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.