IO Dip 502
- Manufacturer
- Ecolab Inc.
- Effective date
- 2025-09-18
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 02:44:59
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SAFE HANDLING WARNING SECTION
FOR INDUSTRIAL USE ONLY
KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE
Wash hands thoroughly after handling. Get medical advice/attention if you feel unwell.
VETERINARY INDICATIONS SECTION
DIRECTIONS:
IMPORTANT: Do not further dilute with water or mix with any other teat dips. If product in dip cup becomes visibly dirty, discard contents and replenish with fresh product. Do not reuse or return any unused product to the original container.
Udder Prep: When using an udder wash step before milking, make sure to wash teats with appropriate udder wash solution using proper cleaning procedures. Teats should then be dried with single-service towels.
Directions for Teat Dipping
Pre-Milk Dipping: Before each cow is milked, and using fresh IO Dip 502, dip each teat full-length into the teat dip cup. Wipe teats after dipping using single-service towels to avoid contamination of milk.
Post-Milk Dipping: Using fresh IO Dip 502, dip each teat full-length into the teat dip cup. Do not wipe. Allow to air dry. Do not turn cows out in freezing weather until the product is completely dry.
Directions for Teat Spraying
Pre-Milk Spraying: Before each cow is milked, and using fresh IO Dip 502, spray entire teat. Wipe teats after dipping using single-service towels to avoid contamination of milk.
Post-Milk Spraying: Using fresh IO Dip 502, spray entire teat immediately after each milking. Do not wipe. Allow to air dry. Do not turn cows out in freezing weather until the product is completely dry.
Expanded Usage: When freshening cows, begin dipping teats twice daily for about 10 days before calving.
PRECAUTION: IO Dip 502 is not intended to cure or help the healing of chapped or irritated teats. As with any germicide, irritation or sensitization may occur in sensitive animals. In case of teat irritation or chapping, have the condition examined and, if necessary, treated by a veterinarian.
Consult your Ecolab representative for specific use instructions and recommended dispensing equipment.
OTHER SAFETY INFORMATION
FIRST AID
IN CASE OF EYE CONTACT: Rinse with plenty of water.
IN CASE OF SKIN CONTACT: Rinse with water.
IF SWALLOWED: Rinse mouth. Get medical attention if symptoms occur.
IF INHALED: Get medical attention if symptoms occur.
READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).
Representative label and principal display panel
A&L Laboratories
IO Dip 502™
Sanitizing Teat Dip
• An aid in reducing the spread of organisms which may cause mastitis
• Contains an emollient system (glycerin and propylene glycol) 5%
• Does not contain Nonylphenol Ethoxylate (NPE)
ACTIVE INGREDIENT:
Iodine ................................................................................................0.5%
INERT INGREDIENTS:.................................................................... 99.5%
TOTAL:............................................................................................... 100.0%
NET CONTENTS: 56.8 L (15 US GAL)
6301345
Manufactured by
Ecolab Inc. · 370 Wabasha Street N · St Paul MN 55102-1390 USA · tel: 1 800 392 3392
© 2015 Ecolab USA Inc. · All rights reserved
Made in United States
760648/5300/0115
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 991290 | iodine 0.5 % Topical Solution | PSN | 3 |
| 1486188 | IoDip-510 0.5 % Iodine Teat Dip | PSN | 3 |
| 1486188 | iodine 5 MG/ML Topical Solution [Iodip] | SBD | 3 |
| 991290 | iodine 5 MG/ML Topical Solution | SCD | 3 |
| 991290 | iodine 0.5 % Topical Solution | SY | 3 |
| 1486188 | Iodip 0.5 % Topical Solution | SY | 3 |
| 1486188 | Iodip 5 MG/ML Topical Solution | SY | 3 |
| 1486188 | IoDip-502 0.5 % Topical Solution | SY | 3 |
| 1486188 | IoDip-505 0.5 % Topical Solution | SY | 3 |
| 1486188 | IoDip-510 0.5 % Topical Solution | SY | 3 |
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 |
|---|---|---|---|---|---|---|
| 47593-533-17 | IO Dip 502 | 56800 mL in 1 DRUM | SOLUTION | 56800 | 3 | |
| 47593-533-21 | IO Dip 502 | 208000 mL in 1 DRUM | SOLUTION | 208000 | 3 | |
| 47593-533-44 | IO Dip 502 | 1150000 mL in 1 PACKAGE | SOLUTION | 1150000 | 3 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| IODINE | ACTIVE INGREDIENT | 9679TC07X4 | 1 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- IO Dip 502
- Iodine
- WATER
- GLYCERIN
- PROPYLENE GLYCOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 47593-533 | 47593-533-44, 47593-533-17, 47593-533-21 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| IODINE | 9679TC07X4 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
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.
