Sodium iodide-Iodine Complex
- Manufacturer
- WestAgro, Inc. | K Klean dba WestAgro, Inc.
- Effective date
- 2015-05-07
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:32:07
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
WARNINGS SECTION
! DANGER
Causes severe eye, skin, and digestive tract burns
SPL UNCLASSIFIED SECTION
FIRST AID
Eyes: Immediately flush with plenty of water at least 15
minutes. If easy to do, remove contact lenses while flushing. Get medical attention immediately.
Skin: Immediately flush with plenty of water at least 15 minutes while removing contaminated clothing. Get medical attention immediately.
If swallowed: DO NOT induce vomiting. Get medical attention immediately. If victim is fully conscious, give a cupful of water. Never give anything my mouth to an unconscious person.
For additional information, consult the Material Safety Data Sheet (MSDS).
SPL UNCLASSIFIED SECTION
DeLaval Manufacturing
11100 N. Congress Ave.
Kansas City, MO 64153
816-891-7700
(M-F, 8:00-4:00 Central Time)
0575-D1109
NET CONTENTS:
LOT NO.:
EXP DATE:
SPL UNCLASSIFIED SECTION
DOT DESCRIPTION
UN1760, Corrosive Liquid,
N.O.S. contains Iodine
Complex), 8, PG II
0575
CORROSIVE 8
CHEMTREC EMERGENCY NO.
1-800-424-9300
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Iodine | ACTIVE INGREDIENT | 9679TC07X4 | 4 | |
| Iodine | ACTIVE MOIETY | 9679TC07X4 | 4 |
Products#
Every source-derived product name is available through these pages.
- Sodium iodide-Iodine Complex
- Iodine
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 33392-575 | 33392-575-99 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Iodine | 9679TC07X4 | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
