Dosage and administration
If necessary, clip hair from area to be treated and cleanse with soap and water. Apply Triodine-7 ® with a swab.
Triodine
- Manufacturer
- Vedco, Inc. | FIRST PRIORITY INCORPORATED
- Effective date
- 2023-06-21
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 02:42:05
Label at a glance#
ProductTriodine
Active ingredientIODINE, POVIDONE-IODINE, POTASSIUM IODIDE
Label structure12 sections
Storage and handling
Store at controlled room temperature between 15°-30°C (59°-86°F). PROTECT FROM LIGHT.
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
ANTISEPTIC/DISINFECTANT
NET CONTENTS:
16 fl oz (473 mL) VINV-TRIO-16OZ
32 fl oz (960 mL) VINV-TRIO-32OZ
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN
INDICATIONS:
For use on cattle, sheep, horses, dogs and swine for topical application on the skin to disinfect superficial wounds, cuts, abrasions, insect bites and minor bruises.
DIRECTIONS FOR USE:
If necessary, clip hair from area to be treated and cleanse with soap and water. Apply Triodine-7® with a swab.
CAUTION:
Not for use in body cavities or deep wounds. Do not use on burns. Do not apply under bandage. Irritation may occur if used on tender skin areas. Avoid contact with eyes and mucous membranes. In case of deep or puncture wounds or serious burns, consult a veterinarian. If redness, irritation, or swelling persists or increases, discontinue use and consult a veterinarian.
STORAGE:
Store at controlled room temperature between 15°-30°C (59°-86°F).
PROTECT FROM LIGHT.
ACTIVE INGREDIENTS:
7% active ingredients provided by Povidone Iodine, Iodine and Potassium Iodide. Provides 2.4% Titratable Iodine*.
INACTIVE INGREDIENTS:
Water, Isopropyl Alcohol and Propylene Glycol.
WARNING:
Ingestion may cause gastrointestinal irritation, nausea and vomiting.
CALL A PHYSICIAN OR POISON CONTROL CENTER.
WARNING! FLAMMABLE! KEEP AWAY FROM HEAT AND OPEN FLAME. KEEP CONTAINER CLOSED WHEN NOT IN USE.
Not For Human Use.
INFORMATION FOR OWNERS/CAREGIVERS SECTION
*Complies with DEA Iodine Regulation 21 C.F.R. §1310.12. No DEA registration required.
Triodine-7 is a registered trademark of First Priority, Inc.
Distributed By
VEDCO, INC.
St. Joseph, MO 64507
16 fl oz (473 mL)
32 fl oz (960 mL)
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 5f30b278-5791-4113-8781-878a9221ef8a | Product name | 2 | 20230125 |
| 2a70c781-a755-4d76-b20a-a958acfbdcdc | Product name | 2 | 20190619 |
| 304592ef-4a8a-4c22-8e8c-af73aa3d60e5 | Product name | 1 | 20180703 |
| ac0821a1-ce75-4ea7-880a-59eecaecdf22 | Product name | 1 | 20180703 |
| db5dc4f9-b907-46f6-8fb7-babcf04bbe5c | Product name | 1 | 20180619 |
| 41e9d6cf-3ed7-4c44-a57e-0685058d0896 | Product name | 1 | 20170824 |
| 5e652c92-68fd-426b-b0e7-5fc64e0b9f99 | Product name | 1 | 20170309 |
| ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c | Product name | 1 | 20150421 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50989-176-26 | Triodine | 12 in 1 CASE | SOLUTION | 12 | 5 | |
| 50989-176-26 | Triodine | 473 mL in 1 BOTTLE, SPRAY | SOLUTION | 473 | 5 | |
| 50989-176-27 | Triodine | 960 mL in 1 BOTTLE | SOLUTION | 960 | 5 | |
| 50989-176-27 | Triodine | 16 in 1 CASE | SOLUTION | 16 | 5 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Triodine
- Triple Source Iodine Tincture
- IODINE
- POVIDONE-IODINE
- POTASSIUM IODIDE
- IODIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50989-176 | 50989-176-26, 50989-176-27 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| IODINE | 9679TC07X4 | ACTIB |
| POVIDONE-IODINE | 85H0HZU99M | ACTIM |
| POTASSIUM IODIDE | 1C4QK22F9J | ACTIM |
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.