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#

ProductIO Dip 502
Active ingredientIODINE
Label structure4 sections

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

PACKAGE LABEL.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

representative labelrepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
991290iodine 0.5 % Topical SolutionPSN3
1486188IoDip-510 0.5 % Iodine Teat DipPSN3
1486188iodine 5 MG/ML Topical Solution [Iodip]SBD3
991290iodine 5 MG/ML Topical SolutionSCD3
991290iodine 0.5 % Topical SolutionSY3
1486188Iodip 0.5 % Topical SolutionSY3
1486188Iodip 5 MG/ML Topical SolutionSY3
1486188IoDip-502 0.5 % Topical SolutionSY3
1486188IoDip-505 0.5 % Topical SolutionSY3
1486188IoDip-510 0.5 % Topical SolutionSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-533-17IO Dip 50256800 mL in 1 DRUMSOLUTION568003
47593-533-21IO Dip 502208000 mL in 1 DRUMSOLUTION2080003
47593-533-44IO Dip 5021150000 mL in 1 PACKAGESOLUTION11500003

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
IODINEACTIVE INGREDIENT9679TC07X41
IODINEACTIVE MOIETY9679TC07X41
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-53347593-533-44, 47593-533-17, 47593-533-21

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
IODINE9679TC07X4ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 11 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IodineIODINENice-Pak Products, LLC857f13fe-51c9-4e5b-b5e2-a981dedabf712026-03-12Warnings, Adverse reactionsName fallback
generic name: IODINE
IodineIODINEUnited Natural Foods, Inc. dba UNFI8e840855-d210-4a99-b73f-6c69dcf2b6fb2026-02-16WarningsName fallback
generic name: IODINE
IODDO IODINEIODINEEVI LABS4af8552c-1f2b-84ad-e063-6394a90abb622026-02-16WarningsName fallback
generic name: IODINE
IodineIODINEWalgreen Co.d3d44c9f-4eb6-4e5b-9943-c0f80f06952d2026-02-12Warnings, Adverse reactionsName fallback
generic name: IODINE
IodiumIODINEBoiron85cd5e7a-52b6-0bb7-e053-2a91aa0aaa142023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd0c27-7859-5fd8-e053-2a91aa0a7c692023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd0c27-782d-5fd8-e053-2a91aa0a7c692023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron724cb010-7c5d-11e6-8589-424c583030312023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd3f96-b800-f192-e053-2991aa0aee982023-02-20Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd5e7a-52a7-0bb7-e053-2a91aa0aaa142023-01-23Name fallback
generic name: IODINE
IodiumIODINEBoiron85ccdc3f-5dd9-a5b1-e053-2a91aa0a8a0c2023-01-05Name fallback
generic name: IODINE

Reported adverse events (FAERS/openFDA)#

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